H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery
NCT: NCT07501949 · NOT_YET_RECRUITING
Brief Summary
The goal of this intent-to-treat study is to evaluate the efficacy of H-Wave Device Stimulation following rotator cuff repair surgery. It is hypothesized that HWDS initiated immediately upon home arrival following rotator cuff repair will not only result in earlier range of motion recovery, but also in better pain relief, medication reduction, sleep quality, and functional recovery. The participants will be randomized into two groups: (a) Routine post-surgical care: standard protocols per procedure, including access to opioid and non-opioid pain medications, (b) Routine post-surgical care plus H-Wave® Device Stimulation (HWDS); and will be followed for 3 months post-surgery.
Frequently Asked Questions
What is H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery?
H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery is a clinical trial registered under NCT07501949. Current status: NOT_YET_RECRUITING.
What is the status of NCT07501949?
The current status of NCT07501949 (H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery) is: NOT_YET_RECRUITING.
When did H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery start?
H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery started on 2026-04-01.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.