Local Anesthesia for Facial Fractures — LAFF  

Pain Management Clinical Trial

Official title: The Impact of Perioperative Nerve Block on Opioid Use After Craniomaxillofacial Trauma Surgery: A Randomized Controlled Trial

Status Recruiting

Clinical Trial Summary

The study is a double-blind randomized, placebo controlled trial examining the impact of perioperative bupivacaine nerve block on PACU recovery metrics. Patients with operative facial fractures are randomized to receive either bupivacaine or saline injections prior to the anesthesia emergence.

Clinical Trial Description

Effective pain management is critical to successful postoperative care and is known to decrease patient morbidity, incurred patient and hospital costs, and length of hospital stay. Pain and nausea after surgery for traumatic facial fractures can limit patients' early morbidity, oral intake, and ability to communicate.

The study is a double-blind randomized, placebo controlled trial examining the impact of perioperative bupivacaine nerve block on PACU recovery metrics. Patients with operative mandibular or midface fractures are randomized to receive either bupivacaine or saline injections prior to the anesthesia emergence. The primary outcome measure is the amount of opioid that patients receive in PACU in morphine milligram equivalent (MMEs).

The purpose of the study is to define whether a perioperative bupivacaine nerve block results in a decrease in the amounts of opioids and antiemetics that patients receive in PACU after CMF trauma surgery. ;

Related Conditions & MeSH terms

• Pain Management

• NCT number: NCT06429501
• Study type: Interventional
• Source: Washington University School of Medicine
• Contact: Amrita Hari-Raj, MD
• Phone: 314-518-6410
• Email: amrita.hari-raj@wustl.edu
• Status: Recruiting
• Phase: Phase 2
• Start date: April 2, 2024
• Completion date: July 1, 2025