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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07485192
Eligibility Criteria:
Inclusion Criteria:
* Patients diagnosed with hemorrhagic or ischemic stroke at least 3 months prior to enrollment.
Patients with shoulder pain of at least 5 cm on the 10-cm Visual Analog Scale (VAS) following hemiplegia.
Patients aged 45-70 years.
Patients with partial tear of the supraspinatus muscle/tendon confirmed by ultrasonographic evaluation.
Exclusion Criteria:
* Patients with limited cooperation.
Patients who received local anesthetic or corticosteroid injection to the shoulder region within the last 3 months.
Patients with a history of surgery or radiotherapy in the shoulder region.
Patients with pre-existing shoulder pain prior to the diagnosis of stroke.
Patients with a cardiac pacemaker.
Patients with malignancy or signs of acute inflammation in the treatment area.
Patients with coagulation disorders or an INR ≥ 4.
Patients with vascular conditions such as deep vein thrombosis, phlebitis, varicose veins, or arterial disease.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
45 Years
Maximum Age:
70 Years
Study:
NCT07485192
Study Brief:
Protocol Section:
NCT07485192