Trials / Withdrawn
WithdrawnNCT06371872
French Cohort of Patients With Rotator Cuff Lesions
French Cohort of Patients With Rotator Cuff Lesions: Changes in Shoulder Function and Quality of Life at 1, 2, 5, 8 and 10 Years, According to Their Care
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to identify, at 5 years, the clinical and therapeutic factors associated with improvement in shoulder functionality and quality of life in patients with transfixing (total) rotator cuff injuries undergoing treatment.
Detailed description
This is a non-interventional, prospective, longitudinal, multicentre cohort study. The research procedure involves recruiting patients during their first consultation for the management of a rotator cuff injury. Patients will then be contacted by telephone or e-mail every year to monitor the progress of their disease and their treatment. Patients will be asked to complete self-questionnaires assessing shoulder function, quality of life and satisfaction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | total transfixing injury to the rotator cuff | develop an appropriate prescription strategy with a view to improving patients' quality of life in the short, medium and long term in this condition |
Timeline
- Start date
- 2025-04-01
- Primary completion
- 2035-12-01
- Completion
- 2035-12-01
- First posted
- 2024-04-17
- Last updated
- 2026-04-01
Source: ClinicalTrials.gov record NCT06371872. Inclusion in this directory is not an endorsement.