Clinical Trials Directory

Trials / Withdrawn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Withdrawn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

TypeNameDescription
PROCEDUREtotal transfixing injury to the rotator cuffdevelop 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.