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 @ 12:54 AM
Ignite Modification Date:
2025-12-25 @ 12:54 AM
NCT ID:
NCT07167667
Eligibility Criteria:
Inclusion Criteria:
* Individuals between the ages of 30-60 who have been diagnosed with CTS by a specialist physician according to international criteria (Those between Stages 1-3),
* Those who have complaints of numbness, tingling, and pain in the first three fingers and half of the fourth finger,
* Phalen Test and Tinel sign or Durkan Test being positive
* Patients who will receive 5 sessions of ESWT application prescribed by a Physical Medicine and Rehabilitation Specialist Physician (for the ESWT group)
* Patients who have been recommended 10 sessions of Paraffin application by a Physical Medicine and Rehabilitation Specialist Physician (for the Paraffin group)
Exclusion Criteria:
* Presence of atrophy in the thenar muscles,
* Insufficient sensory and motor response in the median nerve,
* History of hand and/or wrist injury or surgery,
* Those with cervical stenosis, cervical spondylosis, or cervical radiculopathy,
* Corticosteroids in the carpal tunnel area within the last six months those who have had an injection,
* Pregnancy or diabetes, renal failure, rheumatoid arthritis or hypothyroidism
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
30 Years
Maximum Age:
60 Years
Study:
NCT07167667
Study Brief:
Protocol Section:
NCT07167667