Impact of Anti-inflammatory and Antibiotic Therapy on the Emergence of Peri-tonsillar Abscess

NCT ID: NCT00954031

Last Updated: 2013-01-31

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

TERMINATED

Total Enrollment

711 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-03-31

Study Completion Date

2012-07-31

Brief Summary

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

Analyze in children and adults, risk factors in the onset of the APA. The main hypothesis focuses on the use of anti-inflammatory in the context of pharyngitis or sore throat before the symptoms of ABS. Secondary objectives:

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

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.

Abscess, Peritonsillar

Study Design

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

Observational Model Type

CASE_CONTROL

Study Time Perspective

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

* clinical existence of a PLA (phlegmon), validated by a senior ENT, usually (but not necessarily) following a request by an emergency. The visible appearance to the merits throat must justify puncture. Cases will be included whether or not they had consulted for a "sore throat" in the 10 days preceding the date of diagnosis

Exclusion Criteria

* Neoplastic disease of the throat, scalable Hematologic with tonsillar localization History of tonsillectomy
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Nantes University Hospital

OTHER

Sponsor Role lead

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

Site Status

Angers university Hospital

Angers, , France

Site Status

Caen universty Hospital

Caen, , France

Site Status

Clermont Ferrand University Hospital

Clermont-Ferrand, , France

Site Status

Grenoble University Hospital

Grenoble, , France

Site Status

Lille University Hospital

Lille, , France

Site Status

Ambroise Paré Hospital

Paris, , France

Site Status

Paris-Bichat-Hospital

Paris, , France

Site Status

Paris-Cochin Hospital

Paris, , France

Site Status

Paris-Lariboisière Hospital

Paris, , France

Site Status

Paris-Tenon-Hospital

Paris, , France

Site Status

Poitiers University Hospital

Poitiers, , France

Site Status

Rennes University hospital

Rennes, , France

Site Status

Toulouse University Hospital

Toulouse, , France

Site Status

Tours University Hosipital

Tours, , France

Site Status

Countries

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

France

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.

Outpatient Management of Tonsillectomy in Adults
NCT05915559 ACTIVE_NOT_RECRUITING NA
Intracapsular Tonsillectomy in Adults
NCT03654742 ACTIVE_NOT_RECRUITING NA