ESWT for CRPS-I After Distal Radius Fracture
NCT: NCT07807852 · RECRUITING
Brief Summary
Complex regional pain syndrome type I (CRPS-I) can develop after a distal radius fracture and may cause persistent pain, swelling, limited wrist and hand movement, and difficulty using the affected upper limb. This study will evaluate whether extracorporeal shock wave therapy (ESWT), when added to a standard rehabilitation program, improves symptoms and function in adults with CRPS-I following distal radius fracture. A total of 60 participants will be randomly assigned to one of two groups. Both groups will receive a standard rehabilitation program. One group will also receive active ESWT, while the other group will receive sham ESWT using the same treatment procedure without therapeutic energy delivery. ESWT or sham ESWT will be administered once weekly for five weeks. Participants will be evaluated before treatment, at the end of the 5-week treatment period, and at the 12-week follow-up. The main outcome will be change in pain intensity. Other outcomes will include upper extremity function, wrist range of motion, hand grip strength, and swelling. Adverse events and treatment tolerability will also be recorded.
Frequently Asked Questions
What is ESWT for CRPS-I After Distal Radius Fracture?
ESWT for CRPS-I After Distal Radius Fracture is a clinical trial registered under NCT07807852. Current status: RECRUITING.
What is the status of NCT07807852?
The current status of NCT07807852 (ESWT for CRPS-I After Distal Radius Fracture) is: RECRUITING.
When did ESWT for CRPS-I After Distal Radius Fracture start?
ESWT for CRPS-I After Distal Radius Fracture started on 2026-06-26.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.