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Pericapsular Nerve Group Block (PENG) for Hip Surgery
This will be a randomized comparison of pericapsular nerve group (PENG) blocks with bupivacaine and a placebo control (PENG blocks with normal saline). The overall objective of the proposed research is to determine the relative risks and benefits of a single-injection PENG block to provide postoperative analgesia following hip arthroscopy. Hypothesis 1: Following hip arthroscopy, participants with a PENG block will experience less pain in the recovery room compared with current standard-of-care as measured with the Numeric Rating Scale (NRS). Hypothesis 2: Following hip arthroscopy, participants with a PENG block will consume less opioid in the operating and recovery rooms compared with current standard-of-care as measured in oral morphine milligram equivalents. Primary end point: In order to claim that PENG blocks are superior to placebo overall, at least one of these two hypotheses must demonstrate PENG superiority while the other cannot demonstrate inferiority.
Details
| Lead sponsor | University of California, San Diego |
|---|---|
| Phase | PHASE4 |
| Status | WITHDRAWN |
| Start date | Thu Dec 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Tue May 31 2022 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Hip Arthropathy
- Postoperative Pain, Acute
- Pain, Postoperative
Interventions
- Active bupivacaine 0.375% PENG block
- Placebo normal saline PENG block
Countries
United States