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 @ 2:35 PM
Ignite Modification Date:
2025-12-24 @ 2:35 PM
NCT ID:
NCT05504759
Eligibility Criteria:
Inclusion Criteria:
1. Patients aged 18-65 years with pain in the lateral humeral epicondyle region for at least 6 weeks
2. Patients with pain on palpation of the lateral humeral epicondyle and patients with lateral epicondyle pain manifested by at least one of the provocative tests, such as resistant middle finger extension or resistant wrist extension or passively stretching the wrist extensors
3. Patients with painful trigger points detected by palpation in the extensor group muscles of the forearm
Exclusion Criteria:
1. History of upper extremity trauma or surgery
2. History of arthritis in the upper extremity
3. Patients with EMG-proven entrapment neuropathy in the upper extremity
4. Patients with cervical radiculopathy
5. History of interventional procedures such as physical therapy or steroid injection for lateral epicondylitis in the last 3 months
6. Pregnancy and pregnancy
7. Patients with complaint duration less than 6 weeks
8. Having mental (intelligence-related) problems, limitation of cooperation-orientation (being aware of time and space and having communication skills)
9. \<18 years, \>65 years
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT05504759
Study Brief:
Protocol Section:
NCT05504759