French Cohort of Patients With Rotator Cuff Lesions

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

519 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-04-30

Study Completion Date

2035-12-31

Brief Summary

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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.

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Detailed Description

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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

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Rotator Cuff Injuries

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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patients with rotator cuff injuries

Patients will be recruited during their first consultation for treatment 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. These questionnaires will be accessible via a secure website.

total transfixing injury to the rotator cuff

Intervention Type PROCEDURE

develop an appropriate prescription strategy with a view to improving patients' quality of life in the short, medium and long term in this condition

Interventions

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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

Intervention Type PROCEDURE

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No