Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:12 AM
Ignite Modification Date:
2025-12-25 @ 4:12 AM
NCT ID:
NCT06774820
Eligibility Criteria:
Inclusion Criteria:
* Full-thickness rotator cuff tear of the supraspinatus/infraspinatus tendon, diagnosed preoperatively by ultrasound, arthro-CT or MRI.
* Patients must be able to read and write in French in order to complete the questionnaires and sign the informed consent form.
Exclusion Criteria:
* Partial rotator cuff tear
* Massive and irreparable rotator cuff tear
* Grade 4 according to Goutallier classification of fatty degeneration of rotator cuff muscles
* Rupture of the long biceps
* Hourglass deformity of biceps tendon origin
* Osteoarthritis of the glenohumeral joint, defined by narrowing of the glenohumeral joint space or osteophytes, using AP radiography of the affected shoulder.
* Distance between acromion and humeral head measuring 6 mm or less, defined by Hamada classification as grade 2 or higher.
* Previous shoulder surgery.
* Dementia or inability to complete questionnaires and assessments.
* Pregnant, parturient or breast-feeding patients.
* Persons under legal protection (curatorship, guardianship, safeguard of justice).
* Persons deprived of their liberty by judicial or administrative measure
* Persons under psychiatric care
* Persons not affiliated to a social security scheme
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
40 Years
Study:
NCT06774820
Study Brief:
Protocol Section:
NCT06774820