QL vs PENG for Analgesia After Hip Arthroplasty

Completed · Not applicable

Conditions studied: Block, Hip Replacement, Postoperative Pain

In brief

This study will consist of patients 18 years and older who are undergoing elective hip replacement with planned same day discharge. The patients will be randomized to receive a PENG+LFC or QL block prior to undergoing the surgery to help with postoperative pain control. The primary goal will be assessing postoperative opioid use during the first 72 hours after surgery. Secondary outcomes will include postoperative pain scores from, 0-72 hours. Additional outcomes consist of time to first ambulation, functional and mobility outcomes, PACU duration, patient satisfaction and opioid related side effects.

Key facts

Study ID

NCT05710107

Run by

Medical University of South Carolina

People needed

106

Starts

2023-02-07

Expected to finish

2023-11-12

Last updated by the study team

2024-12-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• age greater than or equal to 18 years of age
• undergoing elective hip arthroplasty with planned same day discharge

You may not qualify if…

• local anesthetic allergy
• subjects with a weight less than 40kg
• subjects that are unable or choose not to give informed consent
• Known preoperative substance abuse

Where it is running

• MUSC — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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