Zynrelef vs Exparel: The Battle of Postoperative Pain Control After Robotic Sleeve Gastrectomy
Zynrelef
+ Exparel
Neurologic Manifestations+4
+ Pain
+ Pain, Postoperative
Treatment Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.130 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy 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
Texas Tech University Health Sciences Center
Lubbock, United StatesOpen Texas Tech University Health Sciences Center in Google Maps