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Clinical Trial

H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery

NCT: NCT07501949 · NOT_YET_RECRUITING

NCT IDNCT07501949
StatusNOT_YET_RECRUITING
Start Date2026-04-01
Completion2027-03-31

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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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