A REAl-life Study on Short-term DAPT in Patients With Ischemic Stroke or TIA

NCT ID: NCT05476081

Last Updated: 2024-12-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

2239 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-02-03

Study Completion Date

2023-05-03

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The REAl-life study on short-term Dual Antiplatelet treatment in Patients with ischemic stroke or Transient ischemic attack (READAPT) is an observational, multicenter, prospective study involving Italian centers. The study aims at evaluating effectiveness and safety of short-term (21-90 days) dual antiplatelet treatment (DAPT) in secondary prevention of mild-to-moderate ischemic stroke or high-risk TIA.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The READAPT will depict the benefit/risk profile of DAPT in a clinical setting, and address subgroups of patients such as those with small cerebral vessel diseases or those treated with revascularization procedures.

Randomized clinical trials (RCTs) proved that short-term DAPT is superior over single antiplatelet treatment in reducing the ischemic recurrence risk, without a remarkable increased hemorrhagic risk thanks to the short treatment course. However, RCTs excluded patients treated with revascularization procedures (i.e. intravenous thrombolysis and thrombectomy), did not provide data on neuroimaging, and had slightly different treatment procedures such as time-to-DAPT start and antiplatelets loading dose.

The study comprises a baseline coinciding with the index event, when the investigators will collect demographics and characteristics of the event, and a 90±5 day follow-up from the index event, when patients will be screened for treatment compliance, tolerability and ischemic or hemorrhagic events. Follow-up visit can be performed remotely.

The investigators did not establish strict NIHSS or ABCD2 score cutoff for patients' inclusion, as treatment decision has to be taken independently from the study, and highly recommend physicians to adhere to guidelines. Each participating center will include all consecutive patients (hospitalized or non-hospitalized) who will meet inclusion criteria.

Data were entered in an electronic anonymized database created on the Research Electronic Data Capture (REDCap) software for the analyses hosted at University of L'Aquila. The local PI or the co-investigators will be able to upload patients' data through a single form specifically created for the study, which will include a user-friendly drop-down menu. Anonymized data will be stored on a secured server under the responsibility of University of L'Aquila. The data will be automatically backed-up once a week. Data will not be shared with unauthorized persons. Plausibility of the entered data will be checked by the study manager and the statistical data manger and data queries will be resolved by Local PI. Cases with missing data or unresolved queries will be rejected to retain only the highest quality data in the registry. Data from centers not ensuring consecutive recruitment of patients or adequate follow-up will not be included in the final database.

All analyses will be performed according to the intention-to-treat principle in all included patients completing the 90-day follow-up or having a fatal outcome event within 90 days. Descriptive statistics will be used to report baseline information. The investigators will analyze the time from index event to the first occurrence of primary and secondary outcome events with the use of a Cox proportional hazards model. Two statistical models will be used: Model 1 unadjusted and Model 2 adjusted for demographics and characteristics of the index event. P values for interaction will be calculated according to the following subgroups: type of event (ischemic stroke vs TIA), time to DAPT (≤24 hours vs \>24 hours from symptom onset), type of DAPT (aspirin+clopidogrel vs aspirin+ticagrelor), DAPT duration (≤21 vs \>21 days and ≤30 vs \>30 days), NIHSS score at onset (≤3 vs \>3 and ≤5 vs \>5), revascularization procedure (i.v. thrombolysis and/or mechanical thrombectomy vs no interventions). Hazard ratios with 95% confidence intervals will be reported. Should multiple events of the same type occur, the time to the first event will be used in the model. Data from patients who had no events during the study will be censored at the time of study termination or death. Assuming a 95% confidence interval, an estimated sample size of 1067 subjects would be required to detect a conservative 50% proportion of primary outcome occurrence with a two-sided 2.5% margin of error.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Ischemic Stroke TIA

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

DAPT Stroke TIA antiplatelet treatment

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients (single cohort study)

Patients presenting with a mild-to-moderate ischemic stroke or high risk TIA

Aspirin

Intervention Type DRUG

Aspirin (100-300 mg) administered for 21-90 days in combination with another antiplatelet treatment

Clopidogrel

Intervention Type DRUG

Clopidogrel (75-600 mg) administered for 21-90 days in combination with another antiplatelet treatment

Ticagrelor

Intervention Type DRUG

Ticagrelor (90-180 mg) administered for 21-90 days in combination with another antiplatelet treatment

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Aspirin

Aspirin (100-300 mg) administered for 21-90 days in combination with another antiplatelet treatment

Intervention Type DRUG

Clopidogrel

Clopidogrel (75-600 mg) administered for 21-90 days in combination with another antiplatelet treatment

Intervention Type DRUG

Ticagrelor

Ticagrelor (90-180 mg) administered for 21-90 days in combination with another antiplatelet treatment

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

B01AC06 acetylsalicylic acid B01AC04 B01AC24

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with mild or moderate non-cardioembolic ischemic stroke or high-risk TIA treated with a short course of DAPT (usually 21-30 days but up to 90-day at the physician's discretion) for the acute event;
* Male or female aged \>18 years;
* Providing signed and dated informed consent;
* Willing to comply with all study procedures and to be available for the duration of the study.

Exclusion Criteria

* Patients receiving DAPT after endovascular procedures with stenting;
* Patients participating to any interventional RCT on stroke prevention;
* Presence of any condition which may preclude reliability of the collected information
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of L'Aquila

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Simona Sacco

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Simona Sacco, MD

Role: STUDY_CHAIR

Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Neurology e Stroke Unit Departement, SS Filippo e Nicola Hospital

Avezzano, Abruzzo, Italy

Site Status

Department of Neurology and Stroke Unit, Ente Ecclesiastico ospedale Generale Regionale Miulli

Acquaviva delle Fonti, , Italy

Site Status

Department f Neurology, AO Nazionale SS Biagio and Cesare Arrigo

Alessandria, , Italy

Site Status

Department of Neurology, Murgia Hospital Fabio Perinei SS 96

Altamura, , Italy

Site Status

Department of Neurology and Stroke Unit Ospedali Riuniti Ancona

Ancona, , Italy

Site Status

Department of Neurology, INRCA-IRCCS "U Sestili" Hospital

Ancona, , Italy

Site Status

Department of Neurology and Stroke Unit, "U. Parini" Hospital

Aosta, , Italy

Site Status

Department of Neurology, San Donato Hospital, Azienda USL Toscana Sud Est, Arezzo e Val D'Arno

Arezzo, , Italy

Site Status

Department of Neurology and Stroke Unit, "Di Venere" Hospital

Bari, , Italy

Site Status

Stroke Unit, Policlinico di Bari, Giovanni XXIII Hospital

Bari, , Italy

Site Status

Department of Neurology and Stroke Unit, "Mons. Dimiccoli" Hospital

Barletta, , Italy

Site Status

Department of Neurology,San Bassiano Hospital

Bassano del Grappa, , Italy

Site Status

Stroke Unit, San Martino di Belluno Hospital ULSS 1

Belluno, , Italy

Site Status

Department of Neurology, AO San Pio

Benevento, , Italy

Site Status

Department of Neurology and Stroke Unit, Maggiore Hospital, IRCCS Istituto delle Scienze Neurologiche di Bologna

Bologna, , Italy

Site Status

Department of Neurology, Policlinico S. Orsola-Malpighi-Clinica Neurologica Metropolitana, IRCCS Istituto delle Scienze Neurologiche di Bologna

Bologna, , Italy

Site Status

Stroke Center, Gubbio-Gualdo Tadino Hospital

Branca, , Italy

Site Status

Neuro-vascular Unit, AO Spedali Civili

Brescia, , Italy

Site Status

Stroke Unit, ASST Franciacorta

Brescia, , Italy

Site Status

Stroke Unit, Istituto Ospedaliero Fondazione Poliambulanza

Brescia, , Italy

Site Status

Stroke Unit, A. Perrino Hospital

Brindisi, , Italy

Site Status

Department of Neurology and Stroke Unit, AO "G. Brotzu"

Cagliari, , Italy

Site Status

Department of Neurology and Stroke Unit, S Elia Hospital

Caltanissetta, , Italy

Site Status

Stroke Unit, AO San Sebastiano AORN Caserta

Caserta, , Italy

Site Status

Department of Neurology, San Giacomo Hospital

Castelfranco Veneto, , Italy

Site Status

Department of Neurology, AO Cannizzaro

Catania, , Italy

Site Status

Department of Neurology, Institute G. Giglio di Cefalù

Cefalù, , Italy

Site Status

Department of Neurology and Stroke Unit, "Bufalini" Hospital

Cesena, , Italy

Site Status

Department of Neurology and Stroke Unit, SS Annunziata Hospital

Chieti, , Italy

Site Status

Department of Neurology and Stroke Unit, Cittadella, AULSS6 Euganea

Cittadella, , Italy

Site Status

Stroke Center, USL umbria 1

Città di Castello, , Italy

Site Status

Stroke Unit, Valduce Hospital

Como, , Italy

Site Status

Department of Neurology, Conegliano Hospital Aulss 2 Veneto

Conegliano, , Italy

Site Status

Department of Neurology and Stroke Unit, ASST Maggiore Hospital of Crema

Crema, , Italy

Site Status

Department of Neurology, ASST Cremona

Cremona, , Italy

Site Status

Department of Neurology, Santa Croce Hospital

Cuneo, , Italy

Site Status

Department of Neurology and Stroke Unit, Desio Hospital ASST Monza

Desio, , Italy

Site Status

Department of Neurology, ASUR Area Vasta 4 (ex ZT11)

Fermo, , Italy

Site Status

Department of NeurologY, AOU of Ferrara

Ferrara, , Italy

Site Status

Department of Neurology, San Giovanni di Dio Hospital

Florence, , Italy

Site Status

Stroke Unit, AOU Careggi

Florence, , Italy

Site Status

Department of Neurology, Ente Ospedali Galliera Genova

Genova, , Italy

Site Status

Stroke Unit, San Martino Hospital of Genova

Genova, , Italy

Site Status

Department of Neurology, ASUGI

Gorizia, , Italy

Site Status

Department of Neurology, USL Toscana sud est

Grosseto, , Italy

Site Status

Department of Neurology and Stroke Unit, ASUR Marche AV2 Jesi

Iesi, , Italy

Site Status

Department of Neuology, Sant'Andrea Hospital, Azienda Sanitaria Locale n. 5 "Spezzino" La Spezia

La Spezia, , Italy

Site Status

Department of Neurology, F Renzetti Hospital

Lanciano, , Italy

Site Status

UTN, Santa Maria Goretti Hospital

Latina, , Italy

Site Status

Department of Neurology, Ospedale Vito Fazi

Lecce, , Italy

Site Status

Department of Neurology, Legnago Hospital

Legnago, , Italy

Site Status

Department of Neurology and Stroke Unit Ospedale of Legnano

Legnano, , Italy

Site Status

Emergency Department, Azienda USL 6 Livorno

Livorno, , Italy

Site Status

Department of Neurology, Valle del Serchio Hospital

Lucca, , Italy

Site Status

Departement of Neurology, San Salvatore Hospital

L’Aquila, , Italy

Site Status

Department of Neurology, Apuane Hospital, Azienda USL Toscana Nord Ovest

Massa, , Italy

Site Status

Department of Neurology, ASST Melegnano e della Martesana

Melegnano, , Italy

Site Status

Department of Neurology, ASST Merate

Merate, , Italy

Site Status

Stroke Unit, AOU Gaetano Martino

Messina, , Italy

Site Status

Stroke Unit, Angelo's Hospital

Mestre, , Italy

Site Status

Stroke Unit, Istituto Clinico Città Studi

Milan, , Italy

Site Status

Department of Neurology and Stroke Unit, Humanitas

Milan, , Italy

Site Status

Department of Neurology and Stroke Unit, IRCCS Istituto Auxologico Italiano, San Luca Hospital

Milan, , Italy

Site Status

Department of Neurology, Mirano ULSS 3 Serenissima

Mirano, , Italy

Site Status

Stroke Unit, "S.Agostino-Estense" Hospital, AOU of Modena

Modena, , Italy

Site Status

Stroke Unit, Santa Croce Hospital

Moncalieri, , Italy

Site Status

Department of Neurology, San Gerardo Hospital and Bicocca University

Monza, , Italy

Site Status

Department of Neurology and Stroke Unit, Cardarelli Hospital

Napoli, , Italy

Site Status

Stroke Unit, Ospedale del Mare

Napoli, , Italy

Site Status

Department of Neurology and Stroke Unit, AOU Maggiore della Carità

Novara, , Italy

Site Status

Stroke Unit, San Giacomo Hospital

Novi Ligure, , Italy

Site Status

Stroke Unit, AOU San Luigi Gonzaga

Orbassano, , Italy

Site Status

Stroke Unit, Azienda Ospedale Università

Padua, , Italy

Site Status

Department of Neurology and Stroke Unit, ARNAS Civico of Palermo

Palermo, , Italy

Site Status

Department of Neurology, Villa Sofia Hospital

Palermo, , Italy

Site Status

Department of Neurophysiopathology and Stroke Unit, AOUP Paolo Giaccone

Palermo, , Italy

Site Status

Stroke Unit, Buccheri La Ferla Hospital

Palermo, , Italy

Site Status

Department of neurology, Azienda Ospedaliero-Universitario di Parma

Parma, , Italy

Site Status

Stroke Unit, Fidenza AUSL PR

Parma, , Italy

Site Status

Cerebrovascula disease and Stroke Unit neurological Intitute IRCCS Mondino

Pavia, , Italy

Site Status

Stroke Unit, AOUUD Santa Maria della Misericordia

Perugia, , Italy

Site Status

Department of Neurology ande Stroke Unit, Pescara Hospital

Pescara, , Italy

Site Status

Stroke Unit, Pederzoli Hospital

Peschiera del Garda, , Italy

Site Status

Department of Neurology, AUSL Piacenza

Piacenza, , Italy

Site Status

Departement of Neurology and Stroke Center, S.Corona Hospital

Pietra Ligure, , Italy

Site Status

Department of Neurology and Stroke Unit, E. Agnelli Hospital

Pinerolo, , Italy

Site Status

Department of Neurology, Azienda ospedaliera e universitaria Pisana

Pisa, , Italy

Site Status

Department of Neurology, San Jacopo Hospital

Pistoia, , Italy

Site Status

Stroke Unit, AO"San Carlo"

Potenza, , Italy

Site Status

Department of Neurology, Maria Paternò Arezzo Hospital

Ragusa, , Italy

Site Status

Department of Neurology and Stroke Unit, Santa Maria delle Croci Hospital

Ravenna, , Italy

Site Status

Stroke Unit, AO "Bianchi-Melacrino-Morelli"

Reggio Calabria, , Italy

Site Status

Department of Neurology and Stroke Unit, Arcispedale Santa Maria Nuova

Reggio Emilia, , Italy

Site Status

Department of Neurology, Infermi di Rimini Hospital

Rimini, , Italy

Site Status

Unità di trattamento neurovascolare, Azienda Ospedaliero Universitaria Policlinico Umberto I

Roma, , Italy

Site Status

Department of Neurology and Stroke Unit, Sant'Eugenio Hospital

Rome, , Italy

Site Status

Department of Neurology and Stroke Unit, Systems Medicin, Policlinico Tor Vergata

Rome, , Italy

Site Status

Department of Neurology, Ospedale Fatebenefratelli

Rome, , Italy

Site Status

Department of Neurology, Policlinico Gemelli

Rome, , Italy

Site Status

Department of Neurology, SS Filippo Neri Hospital

Rome, , Italy

Site Status

Stroke Unit, AO San Camillo

Rome, , Italy

Site Status

Stroke Unit, AOU Sant'Andrea

Rome, , Italy

Site Status

Stroke Unit, Ospedale Rovigo, ULSS 18

Rovigo, , Italy

Site Status

Department of Neurology, Presidio ospedaliero Umberto I Nocera Inferiore

Salerno, , Italy

Site Status

Department of Neurology, Madonna del Soccorso Hospital

San Benedetto del Tronto, , Italy

Site Status

Department of Neurology, ASST Lariana, Sant'Anna Hospital

San Fermo della Battaglia, , Italy

Site Status

Department of Neurology, Casa sollievo della sofferenza

San Giovanni Rotondo, , Italy

Site Status

Stroke Unit, AOU

Sassari, , Italy

Site Status

Department of Neurology, SS. Annunziata Hospital

Savigliano, , Italy

Site Status

Stroke Unit, Azienda ospedaliera universitaria Senese

Siena, , Italy

Site Status

Department of Neurology, SS Annunziata Hospital

Sulmona, , Italy

Site Status

Department of Neurology and Stroke Unit, Umberto I Hospital

Syracuse, , Italy

Site Status

Department of Neurology and Stroke Unit, AO Santa Maria of Terni

Terni, , Italy

Site Status

Department of Neurology and Stroke Unit, San Giovanni Bosco Hospital

Torino, , Italy

Site Status

Neuro-vascular Unit, Maria Vittoria Hospital

Torino, , Italy

Site Status

Department of Neurology and Stroke Unit, ASP of Trapani

Trapani, , Italy

Site Status

Stroke Unit, Santa Chiara Hospital

Trento, , Italy

Site Status

Department of Neurology, Cà Foncello Hospital

Treviso, , Italy

Site Status

Department of Neurology, Azienda Ospedaliera-Universitaria Giuliano Isontina

Trieste, , Italy

Site Status

Department of Neurology and Rehabilitation, ASUR

Udine, , Italy

Site Status

Department of Neurology and Stroke Unit, ASST Settelaghi

Varese, , Italy

Site Status

Department of Neurology, SS Giovanni e Paolo Hospital, Aulss3 Serenissima Veneto

Venezia, , Italy

Site Status

Department of Neurology, Sant'Andrea Hospital

Vercelli, , Italy

Site Status

Department of Neurology and Stroke Unit, Arzignano Azienda ULSS 8 Berica

Vicenza, , Italy

Site Status

Department of Neurology and Stroke Unit, San Bortolo Hospital

Vicenza, , Italy

Site Status

Stroke Unit, ASST Vimercate

Vimercate, , Italy

Site Status

Department of Neurology and Stroke Unit, Guzzardi Hospital

Vittoria, , Italy

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Italy

References

Explore related publications, articles, or registry entries linked to this study.

Wang Y, Wang Y, Zhao X, Liu L, Wang D, Wang C, Wang C, Li H, Meng X, Cui L, Jia J, Dong Q, Xu A, Zeng J, Li Y, Wang Z, Xia H, Johnston SC; CHANCE Investigators. Clopidogrel with aspirin in acute minor stroke or transient ischemic attack. N Engl J Med. 2013 Jul 4;369(1):11-9. doi: 10.1056/NEJMoa1215340. Epub 2013 Jun 26.

Reference Type BACKGROUND
PMID: 23803136 (View on PubMed)

Kennedy J, Hill MD, Ryckborst KJ, Eliasziw M, Demchuk AM, Buchan AM; FASTER Investigators. Fast assessment of stroke and transient ischaemic attack to prevent early recurrence (FASTER): a randomised controlled pilot trial. Lancet Neurol. 2007 Nov;6(11):961-9. doi: 10.1016/S1474-4422(07)70250-8. Epub 2007 Oct 10.

Reference Type BACKGROUND
PMID: 17931979 (View on PubMed)

Johnston SC, Easton JD, Farrant M, Barsan W, Conwit RA, Elm JJ, Kim AS, Lindblad AS, Palesch YY; Clinical Research Collaboration, Neurological Emergencies Treatment Trials Network, and the POINT Investigators. Clopidogrel and Aspirin in Acute Ischemic Stroke and High-Risk TIA. N Engl J Med. 2018 Jul 19;379(3):215-225. doi: 10.1056/NEJMoa1800410. Epub 2018 May 16.

Reference Type BACKGROUND
PMID: 29766750 (View on PubMed)

Johnston SC, Amarenco P, Denison H, Evans SR, Himmelmann A, James S, Knutsson M, Ladenvall P, Molina CA, Wang Y; THALES Investigators. Ticagrelor and Aspirin or Aspirin Alone in Acute Ischemic Stroke or TIA. N Engl J Med. 2020 Jul 16;383(3):207-217. doi: 10.1056/NEJMoa1916870.

Reference Type BACKGROUND
PMID: 32668111 (View on PubMed)

De Santis F, Ornello R, De Matteis E, D'Anna L, Romoli M, Tassinari T, Saia V, Cenciarelli S, Bedetti C, Padiglioni C, Censori B, Puglisi V, Vinciguerra L, Guarino M, Barone V, Zedde M, Grisendi I, Diomedi M, Bagnato MR, Petruzzellis M, Mezzapesa DM, Inchingolo V, Cappellari M, Zivelonghi C, Candelaresi P, Andreone V, Rinaldi G, Bavaro A, Cavallini A, Piscaglia MG, Terruso V, Mannino M, Pezzini A, Frisullo G, Muscia F, Paciaroni M, Mosconi MG, Zini A, Leone R, Palmieri C, Cupini LM, Marcon M, Tassi R, Sanzaro E, Papiri G, Viticchi G, Orsucci D, Falcou A, Beretta S, Tarletti R, Nencini P, Rota E, Sepe FN, Ferrandi D, Caputi L, Volpi G, La Spada S, Beccia M, Rinaldi C, Mastrangelo V, Di Blasio F, Invernizzi P, Pelliccioni G, De Angelis MV, Bonanni L, Ruzza G, Caggia EA, Russo M, Tonon A, Acciarri MC, Anticoli S, Roberti C, Scaglione G, Pistoia F, Fortini A, De Boni A, Sanna A, Chiti A, Barbarini L, Caggiula M, Masato M, Del Sette M, Passarelli F, Bongioanni MR, De Michele M, Ricci S, Sacco S, Foschi M. Real-world outcomes following dual antiplatelet therapy in mild-to-moderate ischemic stroke with anterior versus posterior circulation infarct: a READAPT study propensity matched analysis. Ther Adv Neurol Disord. 2025 Jul 12;18:17562864251351100. doi: 10.1177/17562864251351100. eCollection 2025.

Reference Type DERIVED
PMID: 40661752 (View on PubMed)

De Matteis E, De Santis F, Foschi M, Romoli M, Tassinari T, Saia V, Cenciarelli S, Bedetti C, Padiglioni C, Censori B, Puglisi V, Vinciguerra L, Guarino M, Barone V, Zedde M, Grisendi I, Maestrini I, Bagnato MR, Petruzzellis M, Mezzapesa DM, Di Viesti P, Inchingolo V, Cappellari M, Zenorini M, Candelaresi P, Andreone V, Rinaldi G, Bavaro A, Cavallini A, Moraru S, Piscaglia MG, Terruso V, Mannino M, Pezzini A, Frisullo G, Muscia F, Paciaroni M, Mosconi MG, Zini A, Leone R, Palmieri C, Cupini LM, Marcon M, Tassi R, Sanzaro E, Paci C, Viticchi G, Orsucci D, Falcou A, Diamanti S, Tarletti R, Nencini P, Rota E, Sepe FN, Ferrandi D, Caputi L, Volpi G, La Spada S, Beccia M, Rinaldi C, Mastrangelo V, Di Blasio F, Invernizzi P, Pelliccioni G, De Angelis MV, Bonanni L, Ruzza G, Caggia EA, Russo M, Tonon A, Acciarri MC, Anticoli S, Roberti C, Manobianca G, Scaglione G, Pistoia F, Fortini A, De Boni A, Sanna A, Chiti A, Barbarini L, Caggiula M, Masato M, Del Sette M, Passarelli F, Bongioanni MR, Toni D, Ricci S, Sacco S, Ornello R; READAPT Study Group. Real-World Dual Antiplatelet Therapy Use Exceeds Randomized Trials Boundaries With Possible Safety Issues in Patients With Large Artery Atherosclerosis-Insights From the READAPT Study. Eur J Neurol. 2025 Apr;32(4):e70163. doi: 10.1111/ene.70163.

Reference Type DERIVED
PMID: 40265654 (View on PubMed)

Foschi M, D'Anna L, De Matteis E, De Santis F, Romoli M, Tassinari T, Saia V, Cenciarelli S, Bedetti C, Padiglioni C, Censori B, Puglisi V, Vinciguerra L, Guarino M, Barone V, Zedde M, Grisendi I, Diomedi M, Bagnato MR, Petruzzellis M, Mezzapesa DM, Di Viesti P, Inchingolo V, Cappellari M, Zivelonghi C, Candelaresi P, Andreone V, Rinaldi G, Bavaro A, Cavallini A, Moraru S, Piscaglia MG, Terruso V, Mannino M, Pezzini A, Frisullo G, Muscia F, Paciaroni M, Mosconi MG, Zini A, Leone R, Palmieri C, Cupini LM, Marcon M, Tassi R, Sanzaro E, Papiri G, Paci C, Viticchi G, Orsucci D, Falcou A, Beretta S, Tarletti R, Nencini P, Rota E, Sepe FN, Ferrandi D, Caputi L, Volpi G, La Spada S, Beccia M, Rinaldi C, Mastrangelo V, Di Blasio F, Invernizzi P, Pelliccioni G, De Angelis MV, Bonanni L, Ruzza G, Caggia EA, Russo M, Tonon A, Acciarri MC, Anticoli S, Roberti C, Manobianca G, Scaglione G, Pistoia F, Fortini A, De Boni A, Sanna A, Chiti A, Barbarini L, Caggiula M, Masato M, Del Sette M, Passarelli F, Bongioanni MR, De Michele M, Ricci S, Ornello R, Sacco S; READAPT Study Group. Exploring Sex Differences in Outcomes of Dual Antiplatelet Therapy for Patients With Noncardioembolic Mild-to-Moderate Ischemic Stroke or High-Risk Transient Ischemic Attack: A Propensity-Matched Analysis of the READAPT Study Cohort. Stroke. 2025 Feb;56(2):305-317. doi: 10.1161/STROKEAHA.124.049210. Epub 2024 Dec 9.

Reference Type DERIVED
PMID: 39648888 (View on PubMed)

Ornello R, Foschi M, De Santis F, Romoli M, Tassinari T, Saia V, Cenciarelli S, Bedetti C, Padiglioni C, Censori B, Puglisi V, Vinciguerra L, Guarino M, Barone V, Zedde M, Grisendi I, Diomedi M, Bagnato MR, Petruzzellis M, Mezzapesa DM, Di Viesti P, Inchingolo V, Cappellari M, Zivelonghi C, Candelaresi P, Andreone V, Rinaldi G, Bavaro A, Cavallini A, Moraru S, Querzani P, Terruso V, Mannino M, Pezzini A, Frisullo G, Muscia F, Paciaroni M, Mosconi MG, Zini A, Leone R, Palmieri C, Cupini LM, Marcon M, Tassi R, Sanzaro E, Paci C, Viticchi G, Orsucci D, Falcou A, Beretta S, Tarletti R, Nencini P, Rota E, Sepe FN, Ferrandi D, Caputi L, Volpi G, La Spada S, Beccia M, Rinaldi C, Mastrangelo V, Di Blasio F, Invernizzi P, Pelliccioni G, De Angelis MV, Bonanni L, Ruzza G, Caggia EA, Russo M, Tonon A, Acciarri MC, Anticoli S, Roberti C, Manobianca G, Scaglione G, Pistoia F, Fortini A, De Boni A, Sanna A, Chiti A, Barbarini L, Caggiula M, Masato M, Del Sette M, Passarelli F, Bongioanni MR, Toni D, Ricci S, De Matteis E, Sacco S; READAPT Study Group. Combining Intravenous Thrombolysis and Dual Antiplatelet Treatment in Patients With Minor Ischemic Stroke: A Propensity Matched Analysis of the READAPT Study Cohort. J Am Heart Assoc. 2024 Aug 20;13(16):e036275. doi: 10.1161/JAHA.124.036275. Epub 2024 Aug 9.

Reference Type DERIVED
PMID: 39119964 (View on PubMed)

De Matteis E, De Santis F, Ornello R, Censori B, Puglisi V, Vinciguerra L, Giossi A, Di Viesti P, Inchingolo V, Fratta GM, Diomedi M, Bagnato MR, Cenciarelli S, Bedetti C, Padiglioni C, Tassinari T, Saia V, Russo A, Petruzzellis M, Mezzapesa DM, Caccamo M, Rinaldi G, Bavaro A, Paciaroni M, Mosconi MG, Foschi M, Querzani P, Muscia F, Gallo Cassarino S, Candelaresi P, De Mase A, Guarino M, Cupini LM, Sanzaro E, Zini A, La Spada S, Palmieri C, Sepe FN, Beretta S, Paci C, Caggia EA, De Angelis MV, Bonanni L, Volpi G, Tassi R, Pistoia F, Scoditti U, Tonon A, Viticchi G, Ruzza G, Nencini P, Cavallini A, Toni D, Ricci S, Sacco S; READAPT Study Group. Divergence Between Clinical Trial Evidence and Actual Practice in Use of Dual Antiplatelet Therapy After Transient Ischemic Attack and Minor Stroke. Stroke. 2023 May;54(5):1172-1181. doi: 10.1161/STROKEAHA.122.041660. Epub 2023 Mar 23.

Reference Type DERIVED
PMID: 36951052 (View on PubMed)

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

03/2021

Identifier Type: -

Identifier Source: org_study_id