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Zynrelef vs Exparel: The Battle of Postoperative Pain Control After Robotic Sleeve Gastrectomy

NCT06349772 · Texas Tech University Health Sciences Center · Updated 8 July 2026

What is being tested
Zynrelef; Exparel
For
Post Operative Pain
Kind of study
Tests a treatment or device on volunteers. Early phase 1.
Who can join
Ages 18 years to 65 years. About 130 people. The full rules are on the registry page.
Where
United States
When
Starts or started 1 Nov 2024, ends 1 Dec 2028. Registered 5 April 2024.
Results
None posted yet.

In the researchers' words

The purpose of this study is to evaluate the use of an injectable combination of bupivacaine and meloxicam (Zynrelef) vs injectable liposomal bupivacaine (Exparel), two extended local anesthesia strategies currently approved by FDA and on the market for post-surgical pain control. The investigators plan on randomizing study participants to either Exparel or Zynrelef at the closure site of robotic sleeve gastrectomy and assessing their pain control postoperatively both in the hospital and at home. The investigators will measure the outcome of two drugs, Zynrelief, and Exparel on postoperative pain score -using the NRS pin score up to 72 hours after surgery. The total opioid use will be recorded in forms that will be used to measure pain score and total opioid use and will be collected to the Excel sheet. The cost of the drug will be calculated for internal use for Hospital purpose only.
ClinicalTrials.gov, NCT06349772

Sites

  • Texas Tech University Health Sciences CenterLubbock, Texas, United States