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:
2025-12-24 @ 4:12 PM
Ignite Modification Date:
2025-12-24 @ 4:12 PM
NCT ID:
NCT07086066
Eligibility Criteria:
Inclusion Criteria:
Individuals aged between 25 and 55
Individuals diagnosed with a rotator cuff injury through radiological methods
Individuals experiencing severe pain (VAS ≥ 3) and functional loss
Individuals who are willing to participate in the study and have signed the written informed consent form after understanding the purpose and procedure of the study
Exclusion Criteria:
Individuals with a history of rotator cuff surgery
Individuals with a history of shoulder subluxation
Individuals with a history of SLAP lesions
Individuals with respiratory system diseases
Individuals with nerve damage (e.g., brachial plexus lesions) or neurological disorders that may affect shoulder movements
Individuals with psychological disorders (e.g., depression, anxiety) that may affect pain perception
Pregnant or breastfeeding women
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
25 Years
Maximum Age:
55 Years
Study:
NCT07086066
Study Brief:
Protocol Section:
NCT07086066