Impact of Anti-inflammatory and Antibiotic Therapy on the Emergence of Peri-tonsillar Abscess
NCT ID: NCT00954031
Last Updated: 2013-01-31
Study Results
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.
TERMINATED
711 participants
OBSERVATIONAL
2009-03-31
2012-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
1. \- Analyze the implementation of a rapid diagnostic test and its result on the occurrence of an ABS
2. \- Measure the frequency of prescription and describe the reasons for not prescribing an antibiotic for patients who consulted for a sore throat and having developed a PLA
3. \- Describe the microbial flora could puncture of patients hospitalized for APA
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Medical Versus Surgical Treatment for Peritonsillar Abscesses
NCT04998513
Surgical Treatment of Tonsillar Abscess
NCT04543708
Peritonsillar Abscess: Aspiration Versus Tonsillectomy a Chaud
NCT03326661
Role of Antibiotics Post Tonsillectomy
NCT03491085
Investigation of Clinical Spectrum, Bacterial Pathogens and Immune Response in Acute Pharyngotonsillitis
NCT00926198
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
case
hospitalized patients, adult or child, including the diagnosis of APA was made, after consulting their physician.
No interventions assigned to this group
The control group
Two patients witnesses will be matched to each case:
Chronological criterion: consultation for a "sore throat" 10 days (± 3 days) before the date of hospitalization of cases, between 13 and J-J-7.
Age criteria: year of birth ± 5 years Geographical criteria: living in the same department, failing in an adjacent Department Social criteria: beneficiary or otherwise of the CMU, to avoid a selection bias leading social most frequently at the onset of the APA
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Nantes University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nantes University Hospital
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Gilles Potel, PhD
Role: PRINCIPAL_INVESTIGATOR
Nantes University Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Nantes University Hospital
Nantes, Pays de Loire, France
Angers university Hospital
Angers, , France
Caen universty Hospital
Caen, , France
Clermont Ferrand University Hospital
Clermont-Ferrand, , France
Grenoble University Hospital
Grenoble, , France
Lille University Hospital
Lille, , France
Ambroise Paré Hospital
Paris, , France
Paris-Bichat-Hospital
Paris, , France
Paris-Cochin Hospital
Paris, , France
Paris-Lariboisière Hospital
Paris, , France
Paris-Tenon-Hospital
Paris, , France
Poitiers University Hospital
Poitiers, , France
Rennes University hospital
Rennes, , France
Toulouse University Hospital
Toulouse, , France
Tours University Hosipital
Tours, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BRD 08/9-W
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.