French Cohort of Patients With Rotator Cuff Lesions

Launched by GCS RAMSAY SANTÉ POUR L'ENSEIGNEMENT ET LA RECHERCHE · Apr 15, 2024

Keywords

ClinConnect Summary

This clinical trial is looking to understand how different factors affect the recovery of patients with severe shoulder injuries known as transfixing rotator cuff lesions. Specifically, the study aims to see how these injuries impact shoulder function and quality of life after five years of treatment. By gathering information from participants, researchers hope to identify what helps people improve their shoulder health and overall well-being.

To be eligible for this study, participants must be adults aged 18 and older with a confirmed diagnosis of a total rotator cuff injury. They should also be able to communicate and provide feedback through online questionnaires. However, older adults over 75, those who have had previous shoulder surgeries, or individuals unable to participate due to legal protections will not be included. If you join the trial, you can expect to share your experiences and complete some online surveys about your shoulder function and daily life. This research aims to help improve treatment options for future patients with similar injuries.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patient, male or female, over 18 years of age.
• • Patient with a transfixing (total) rotator cuff lesion confirmed by imaging.
• • A patient who has been informed and has expressed no oral objection to taking part in the research.
• • Patient affiliated to or benefiting from a social security scheme.
• Exclusion Criteria:
• • Patients over 75 years of age.
• • Patients with a history of shoulder surgery.
• • Patients unable to receive emails and/or answer online questionnaires.
• • Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.