At a glance
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Evaluation of Bridge Device in Pain Management for Outpatient Rotator Cuff Surgery
In Brief
A clinical study evaluating Bridge Percutaneous Nerve Field Stimulator for Pain and Rotator Cuff Injuries. Completed, enrolled 42 participants across 1 site.
Detailed Summary
The objective of the trial is to investigate the efficacy of the Bridge device in reducing post-operative pain and post-operative opioid consumption in patients undergoing rotator cuff surgery with the typical mode of anesthesia, nerve block plus propofol sedation.
Study Details
Timeline
Interventions
The Bridge device is an FDA-cleared, drug-free, non-surgical device that uses neuro-modulation to aid in the reduction of symptoms associated with opioid withdrawal through application to branches of the Cranial Nerves V, VII, IX, X, and the occipital nerves. This study is investigating its effectiveness treating post-surgical pain.