Comparing pain management methods after sleeve gastrectomy
Postoperative Analgesia in Laparoscopic Sleeve Gastrectomies: Laparoscopic Versus Ultrasound-guided Transversus Abdominis Plane Block
Biruni University · NCT06253208
This study is testing two different ways to manage pain after weight loss surgery to see which one works better for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Biruni University (other) |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06253208 on ClinicalTrials.gov |
What this trial studies
This study compares two different methods of analgesia for patients undergoing laparoscopic sleeve gastrectomy, focusing on postoperative pain management in the first 24 hours after surgery. It aims to evaluate the effectiveness of laparoscopic versus ultrasound-guided block techniques in alleviating pain for morbidly obese patients. Given the rising number of obesity surgeries, understanding optimal pain management strategies is crucial for improving patient outcomes and minimizing complications. The study will involve patients who meet specific inclusion criteria, ensuring a targeted approach to pain management.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old with a BMI greater than 30 who can tolerate general anesthesia.
Not a fit: Patients with serious underlying health conditions, chronic pain, or those who are pregnant may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved postoperative pain management strategies for patients undergoing bariatric surgery.
How similar studies have performed: Previous studies have shown varying success with different analgesia methods in postoperative settings, but this specific comparison is less commonly explored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who can tolerate general anesthesia and pneumoperitoneum. * Patients who can give informed consent for surgery. * Patients over 18 years of age * patients with body mass index (BMI) \> 30 kg/m2 * Patients with American Society of Anesthesiologists (ASA) physical status I and II Exclusion Criteria: * Patients allergic to local anesthetics. * Patients with serious underlying cardiovascular disease (e.g. congestive heart failure, conduction disorders and ischemic heart disease). * Patients with chronic kidney disease stage 3 or greater (creatinine clearance less than 60 mL/min). * Patients who have had previous abdominal surgery, including resection of the esophagus, stomach, liver and pancreas. * Patients with chronic pain and chronic opioid use * Patients with ASA class IV * patients with psychiatric disorders * pregnant or breastfeeding patients * patients with a history of seizures
Where this trial is running
Istanbul
- Istinye University — Istanbul, Turkey (RECRUITING)
Study contacts
- Study coordinator: ilke dolgun
- Email: ilkeser2004@gmail.com
- Phone: +905555485632
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Postoperative Pain