Recruiting

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

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Zynrelef

+ Exparel

Drug
Who is being recruted

Neurologic Manifestations+4

+ Pain

+ Pain, Postoperative

From 18 to 65 Years
+14 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Early Phase 1
Interventional
Study Start: November 2024
See protocol details

Summary

Principal SponsorTexas Tech University Health Sciences Center
Study ContactTommy Wright, DOMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 1, 2024

Actual date on which the first participant was enrolled.

This study is focused on comparing two different medicines, Zynrelef and Exparel, which are used to manage pain after surgery. Specifically, it looks at people who have undergone robotic sleeve gastrectomy, a type of weight-loss surgery. The goal is to see which medicine is better at controlling pain after the operation. Both Zynrelef, which combines bupivacaine and meloxicam, and Exparel, a liposomal form of bupivacaine, are already approved by the FDA for pain relief after surgery. Understanding which option controls pain more effectively could help improve recovery and reduce the need for additional pain medication, such as opioids, which can have side effects. Participants in the study will be randomly assigned to receive either Zynrelef or Exparel at the site where their surgery incisions are closed. The study will assess how well these medicines manage pain by using a pain rating scale over the first 72 hours after the surgery, both while in the hospital and at home. Additionally, the study will track how much opioid medication is used by participants, as reducing opioid use is beneficial for recovery. The cost of each drug will also be analyzed for the hospital's internal purposes, although this information will not affect the participants directly. Overall, this study aims to find the most effective way to manage pain after sleeve gastrectomy surgery.

Official TitleZynrelef vs Exparel: The Battle of Postoperative Pain Control After Robotic Sleeve Gastrectomy
NCT06349772
Principal SponsorTexas Tech University Health Sciences Center
Study ContactTommy Wright, DOMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

130 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainPain, PostoperativePathologic ProcessesPostoperative ComplicationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Criteria

4 inclusion criteria required to participate
Age range: 18-65 years old

Scheduled or being scheduled to undergo robotic sleeve gastrectomy by Dr. Goyal.

Is able to provide written informed consent.

Is able to adhere to the study visit schedule and complete all study assessments.

10 exclusion criteria prevent from participating
Positive urine drug screen prior to surgery

History of substance abuse in the past year-by self report

Patient with ongoing daily narcotic use at the time of surgery-by self report

Inability to understand informed consent or read English/Spanish

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Those who get zynrelef injected at the at the 12mm port incision

Group II

Experimental
those who get exparel injected at the 12mm port incision

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Texas Tech University Health Sciences Center

Lubbock, United StatesOpen Texas Tech University Health Sciences Center in Google Maps
Recruiting
One Study Center