Observational analysis of patients with thoracic outlet syndrome
Evaluation Des Mesures Dopplers, Angiographiques, Radiographique Oximetriques, Plethysmographiques, Electromyographiques et Des Questionnaires Cliniques Des Patients adressés Pour Suspicion de Syndrome du défilé Thoraco-brachial
This study looks at patients who might have thoracic outlet syndrome to gather information about their symptoms and test results to better understand and manage the condition.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Angers Government |
| Locations | 1 site (Angers) |
| Trial ID | NCT04376177 on ClinicalTrials.gov |
What this trial studies
This study involves the collection and analysis of data from patients suspected of having thoracic outlet syndrome (TOS). It records various patient characteristics, symptoms, and results from multiple diagnostic tests, including photoplethysmography, transcutaneous oximetry, and imaging studies. The goal is to create a comprehensive database that can help in understanding the condition and improving diagnosis and management. The study is observational, meaning it does not involve any experimental interventions but rather focuses on existing clinical practices.
Who should consider this trial
Good fit: Ideal candidates for this study are patients referred for suspected thoracic outlet syndrome who can provide consent for the use of their medical files.
Not a fit: Patients who are unable to understand the purpose of the database or are protected by law may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding and management of thoracic outlet syndrome, leading to better patient outcomes.
How similar studies have performed: While this study is observational and focuses on data collection, similar approaches in other conditions have shown success in improving diagnostic accuracy and patient management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Absence of deny for the use of medical filesfor research purposes Exclusion Criteria: * Inability to understand the purpose of the database. * Patient protected by law.
Where this trial is running
Angers
- University Hospital — Angers, France (Recruiting)
Study contacts
- Principal investigator: Pierre ABRAHAM, MD; PhD — University and univerity hospital in Angers, FRANCE
- Study coordinator: pierre Abraham, MD PhD
- Email: piabraham@chu-angers.fr
- Phone: +33241353689
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.