Evaluating quality of life after surgery for thoracic outlet syndrome
Differences in Quality of Life After Thoracic Outlet Syndrome Surgery
This study is trying to see how surgery for thoracic outlet syndrome affects the daily lives and well-being of adults who have the procedure.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 112 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Angers Government |
| Locations | 1 site (Angers) |
| Trial ID | NCT05426473 on ClinicalTrials.gov |
What this trial studies
This study evaluates the quality of life in patients who have undergone surgery for thoracic outlet syndrome. It utilizes the QuickDASH and SF-36 forms to assess patient outcomes post-surgery. The focus is on understanding how surgical intervention impacts daily functioning and overall well-being. The study is conducted at the University Hospital in Angers, targeting adult patients who are scheduled for this specific surgical procedure.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who are scheduled for thoracic outlet syndrome surgery and understand French.
Not a fit: Patients who are unable to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of surgical treatment for improving quality of life in patients with thoracic outlet syndrome.
How similar studies have performed: While there may be studies evaluating quality of life post-surgery for various conditions, this specific focus on thoracic outlet syndrome surgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * thoracic outel syndrome surgery scheduled in the vascular and thoracic surgery department of Angers ; age \> 18 y ; french language understood Exclusion Criteria: * denied of consent
Where this trial is running
Angers
- University Hospital — Angers, France (Recruiting)
Study contacts
- Study coordinator: Eva Deveze, Dr
- Email: Eva.Deveze@chu-angers.fr
- Phone: 0686450820
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.