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French Cohort of Patients With Rotator Cuff Lesions

NCT06371872 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2026-04-01

No results posted yet for this study

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.

Conditions

  • Rotator Cuff Injuries

Interventions

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

Sponsors & Collaborators

  • Euraxi Pharma

    collaborator INDUSTRY

  • GCS Ramsay Santé pour l'Enseignement et la Recherche

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-30
Primary Completion
2035-12-31
Completion
2035-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06371872 on ClinicalTrials.gov