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Efficacy of Pericapsular Nerve Group (PENG) Block on Postoperative Pain Management After Acetabular Fracture Fixation: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to find out whether a Pericapsular Nerve Group (PENG) block, a type of nerve block used to control pain, can reduce pain after surgery in adults with an acetabular (hip socket) fracture who are undergoing surgical repair. The study will also evaluate the safety of the PENG block. The main questions this study aims to answer are: Does a PENG block reduce pain after surgery? Does a PENG block reduce the need for opioid pain medications after surgery? Are there any side effects or complications related to the PENG block? Researchers will compare patients who receive a PENG block with patients who do not receive a PENG block to determine whether the block improves pain control after surgery. Participants will: Be randomly assigned to receive either a PENG block or no PENG block before surgery while under general anesthesia. Undergo surgery to repair their acetabular fracture. Receive the same standard pain medications after surgery. Be asked to rate their pain at several time points after surgery using a standard pain scale. Have their use of pain medications, recovery, and any side effects recorded during their hospital stay and follow-up.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient age 18 years or older

• Acetabular Fracture amenable to surgery through the Kocher-Langenbeck approach

• Full weight-bearing capacity prior to the trauma

• Providing written informed consent

Locations
Other Locations
Puerto Rico
Puerto Rico Medical Center
RECRUITING
San Juan
Time Frame
Start Date: 2025-09-08
Estimated Completion Date: 2027-03-30
Participants
Target number of participants: 70
Treatments
Experimental: PENG Block Group
This group includes participants who will receive the pericapsular nerve group (PENG) block after surgical intervention.
No_intervention: NO PENG Block Group
This group includes participants who will not receive the pericapsular nerve group (PENG) block after surgical intervention and will be considered our control group.
Related Therapeutic Areas
Sponsors
Leads: University of Puerto Rico

This content was sourced from clinicaltrials.gov

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