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French Cohort of Patients With Rotator Cuff Lesions (PRO-CUFF)

G

GCS Ramsay Santé pour l'Enseignement et la Recherche

Status

Not yet enrolling

Conditions

Rotator Cuff Injuries

Treatments

Procedure: total transfixing injury to the rotator cuff

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06371872
2024-A00173-44

Details and patient eligibility

About

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.

Full 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.

Enrollment

519 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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.

Trial design

519 participants in 1 patient group

patients with rotator cuff injuries
Description:
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.
Treatment:
Procedure: total transfixing injury to the rotator cuff

Trial contacts and locations

1

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Central trial contact

Geoffroy NOURISSAT, MD

Data sourced from clinicaltrials.gov

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