Italian PheNotypes Obstructive Sleep Apnea Study

NCT ID: NCT06872242

Last Updated: 2025-03-12

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

RECRUITING

Total Enrollment

5000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-06-01

Study Completion Date

2025-10-23

Brief Summary

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

Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.

Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database) , a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.

The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).

Aims of the present project are to:

1. Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
2. Analyze the association between OSA and co-morbidities
3. implementation of an "Italian database" for long-term follow-up studies.

Methods

* Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center).
* Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening
* A web-based data collection platform will be designed to store pseudo-anonymized individual data.

OUTCOMES

1. Distribution of OSA severity in Italy according to the different classification methods
2. Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
3. Distribution of different physiological and clinical patterns and their association with co-morbidities
4. Definition of a screening/case finding questionnaire for Italian Population
5. Definition of an ongoing cohort of patients that will be followed-up
6. Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.

Detailed Description

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

Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.

Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database), a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.

The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).

Aims of the present project are to:

1. Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
2. Analyze the association between OSA and co-morbidities by taking into account the phenotypes already described in the literature, i.e., ESADA, Icelandic Sleep Cohort, and BAVENO classification;
3. implementation of an "Italian database" for long-term follow-up studies. The project will set an HUB and SPOKE organization that include 4 leading research Sleep Center distributed over the Italian territory in collaboration with the Italian Scientific Society of Sleep Medicine (AIMS) network. AIMS is member of the European Federation of National Sleep Society as well as part of World Sleep Association.

Methods

* Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center). Additional clinical tests will include: EKG, Spirometry, ABPM, standard blood chemistry, CPR, TSH reflex, glycemic control assesment, Vitamin D and B12.
* Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening will be performed by means of ESS, MOCA and HADS, respectively
* A web-based data collection platform will be designed to store pseudo-anonymized individual data.

OUTCOMES

1. Distribution of OSA severity in Italy according to the different classification methods (AHI based; hypoxic burden; Icelandic Sleep Cohort, ESADA and BAVENO method)
2. Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
3. Distribution of different physiological and clinical patterns and their association with co-morbidities; analysis of differences with other populations.
4. Definition of a screening/case finding questionnaire for Italian Population
5. Definition of an ongoing cohort of patients that will be followed-up
6. Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.

Conditions

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

Sleep Apnea

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

CROSS_SECTIONAL

Study Groups

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

Patients with suspected obstructive sleep apnea (OSA)

Patients referred to the Italian Sleep Centres because of suspected OSA

Polysomnography

Intervention Type DIAGNOSTIC_TEST

Polysomnography after enrollment for suspected obstructive sleep apnea

Interventions

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

Polysomnography

Polysomnography after enrollment for suspected obstructive sleep apnea

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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

Inclusion Criteria

* Suspected Obstructive Sleep Apnea
* Age 18 years or older

Exclusion Criteria

* Unstable psychiatric disease
* Limited life expectancy due to illness unrelated to sleep apnoea or other medical conditions which may interfere with the study protocol in the opinion of the investigator
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.

Istituto Auxologico Italiano

OTHER

Sponsor Role lead

Responsible Party

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

Responsibility Role SPONSOR

Locations

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

ASP Cosenza- PO Beato Angelico

Acri, , Italy

Site Status RECRUITING

AOU delle Marche

Ancona, , Italy

Site Status NOT_YET_RECRUITING

AOU Policlinico di Bari

Bari, , Italy

Site Status RECRUITING

ASST Papa Giovanni XXIII

Bergamo, , Italy

Site Status RECRUITING

Casa di cura San Francesco-Istituto Madre Rubatto

Bergamo, , Italy

Site Status RECRUITING

AUSL Bologna - Clinica odontoiatrica DIBINEM

Bologna, , Italy

Site Status ACTIVE_NOT_RECRUITING

AUSL Bologna - Ospedale di Bellaria

Bologna, , Italy

Site Status NOT_YET_RECRUITING

AOU Cagliari - Centro interdipartimentale dei disturbi del sonno

Cagliari, , Italy

Site Status RECRUITING

AOU Rodolico-S. Marco

Catania, , Italy

Site Status NOT_YET_RECRUITING

ASP Cosenza- P.O. di Rossano

Corigliano-Rossano, , Italy

Site Status RECRUITING

Distretto Sanitario Cosenza- Savuto- Ambulatorio di Medicina del Sonno

Cosenza, , Italy

Site Status RECRUITING

AOU Ospedali Riuniti di Foggia

Foggia, , Italy

Site Status RECRUITING

Opera Don Uva Universo Salute

Foggia, , Italy

Site Status RECRUITING

IRCCS Ospedale Policlinico San Martino

Genova, , Italy

Site Status NOT_YET_RECRUITING

Ospedale Carlo Urbani

Iesi, , Italy

Site Status NOT_YET_RECRUITING

IRCCS Istituto Neurologico "Carlo Besta"

Milan, , Italy

Site Status RECRUITING

Istituto Auxologico Italiano

Milan, , Italy

Site Status RECRUITING

Ospedale San Paolo

Milan, , Italy

Site Status RECRUITING

AO dei Colli - PO Monaldi

Napoli, , Italy

Site Status NOT_YET_RECRUITING

Ospedali Riuniti Villa Sofia Cervello

Palermo, , Italy

Site Status RECRUITING

Azienda Ospedaliero-Universitaria di Parma

Parma, , Italy

Site Status NOT_YET_RECRUITING

IRCCS Fondazione Mondino

Pavia, , Italy

Site Status RECRUITING

Istituti Clinici Scientifici Maugeri

Pavia, , Italy

Site Status RECRUITING

Casa di Cura "Villa Serena"

Pescara, , Italy

Site Status NOT_YET_RECRUITING

Azienda Ospedaliero-Universitaria Pisana

Pisa, , Italy

Site Status RECRUITING

IRCCS Neuromed - Istituto Neurologico Mediterraneo

Pozzilli, , Italy

Site Status RECRUITING

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Roma, , Italy

Site Status NOT_YET_RECRUITING

Policlinico Tor Vergata

Roma, , Italy

Site Status NOT_YET_RECRUITING

AOU Città della Salute e della Scienza di Torino - SC Otorinolaringoiatria

Torino, , Italy

Site Status NOT_YET_RECRUITING

USL Umbria1 - Ambulatorio disturbi del sonno

Umbertide, , Italy

Site Status RECRUITING

Countries

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

Italy

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Carolina Lombardi, PhD

Role: CONTACT

+3902619111 ext. 2750

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Maria Ferraro

Role: primary

+390982 581264

Antonina Re

Role: primary

+390715964338

Elisiana Carpagnano

Role: primary

+3908055922907

Maria Cristina Servalli

Role: primary

+390352673296

Anna Micheli

Role: primary

+393385327017

Federica Provini

Role: primary

+390514966990

Stefania Redolfi

Role: primary

070 675 3113

Alberto Bianchi

Role: primary

+393357067060

Miguel Angel Paludi

Role: primary

+393392033505

Paola Elisa Scarpino

Role: primary

+3909848934852

Pasquale Tondo

Role: primary

+393925078524

Maria Pia Foschino Barbaro

Role: primary

+393204394764

Dario Arnaldi

Role: primary

+39105557130

Alessia Resedi

Role: primary

+390717130723

Giuseppe Didato

Role: primary

02 23942576

Carolina Lombardi

Role: primary

+3902619112750

Elena Zambrelli

Role: primary

+39 02 81844201

Marialuisa Bocchino

Role: primary

+393334914670

Maria Rosaria Bonsignore

Role: primary

+3909123869203

Liborio Parrino

Role: primary

+390521704107

Michele Terzaghi

Role: primary

0382 380335

Francesco Fanfulla

Role: primary

+390382592807

Biancamaria Guarnieri

Role: primary

090 2212289

Enrica Bonanni

Role: primary

+39050992088

Andrea Romigi

Role: primary

+3908659291

Valerio Brunetti

Role: primary

0630154304

Claudio Liguori

Role: primary

+390620903132

Giuseppe Riva

Role: primary

+393335865851

Chiara Bedetti

Role: primary

+390758935307

Other Identifiers

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

09M205

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.