PENG Block Versus LP Block for THA Postop Pain

• Status: Not yet recruiting
• Trial end date: 2024-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this randomized, double blinded, prospective study is to compare the postoperative analgesia provided by the PENG block to that provided by the LPB for patients undergoing primary anterior approach THA.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Wake Forest University Health Sciences

Criteria

Inclusion Criteria:

elective primary total hip arthroplasty surgery anterior approach provided informed consent no contraindications to medications used in providing the analgesic blocks

Exclusion Criteria:

contraindications to regional anesthesia, such as an allergy to amide local anesthetics pre-existing coagulopathy or thrombocytopenia <100,000 refusal of analgesic block for pain management presence of an progressive lower extremity neurological deficit localized or systemic infection chronic use of high dose opioid analgesics (defined as daily use greater than 60 mg oxycodone equivalents) pregnant refusal of consent