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 @ 2:10 AM
Ignite Modification Date:
2025-12-25 @ 2:10 AM
NCT ID:
NCT01587560
Eligibility Criteria:
Inclusion Criteria:
* Primary or secondary osteoarthritis of the shoulder
* Age 40-75 years
* Patient capable of giving informed consent
* Patient agrees to comply with the study plan
Exclusion Criteria:
* Destruction of the proximal humerus
* Insufficient bone stock
* Deficient rotator cuff or earlier failed surgery of the rotator cuff
* Large muscle defects or insufficient blood supply in the affected arm
* Neuromuscular disorders
* Infection, untreated malignancy or transmittable disease preventing the patient from fulfilling the study
* Patient unwilling to comply with study regulations
* Patient with earlier allergic reaction to pyrocarbon
* Patient with known metastatic disease
* Patient who has been treated with more than 10 mg corticosteroids (e.g. Prednisone) daily within 3 months from surgery.
* Patient participating in other clinical study
* Patient in need of glenoid replacement
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
40 Years
Maximum Age:
75 Years
Study:
NCT01587560
Study Brief:
Protocol Section:
NCT01587560