Comparing recovery methods after laparoscopic sleeve gastrectomy
Official title: Quality of Recovery in Laparoscopic Sleeve Gastrectomy Using Dexmedetomidine Infusion Versus Laparoscopic TAP Block in Combination With Paragastric Neural Block
Run by Alexandria University · NCT06970626 · Data updated 2026-11-12
This study is testing which recovery method works better for people with obesity after laparoscopic sleeve gastrectomy by comparing two different pain management techniques.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Ages | 20 Years to 60 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Alexandria University Academic / other |
| Locations | 1 site (Alexandria) |
| Status | Recruiting |
| Started | April 3, 2025 |
| Main results expected | June 4, 2025 |
| Study ends | June 20, 2025 |
| Registry record updated | May 14, 2025 |
| Trial ID | NCT06970626 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients with a BMI between 35 and 50 kg/m2 and classified as ASA physical status II-III.
✕Probably not a fit
Patients with significant hepatic, renal, neuromuscular, or cardiac impairments, extreme obesity (BMI > 50 kg/m2), or those currently on opioid medication may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial aims to determine which recovery method is more effective for patients undergoing laparoscopic sleeve gastrectomy: a combination of dexmedetomidine infusion and paragastric neural block or a combination of laparoscopic TAP block and paragastric neural block. The study will evaluate recovery by measuring opioid consumption, hemodynamic stability, pain scores, quality of postoperative recovery, and incidence of nausea or vomiting. It involves patients with a BMI of 35-50 kg/m2 and ASA physical status II-III, assessing their recovery outcomes post-surgery.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery protocols for patients undergoing laparoscopic sleeve gastrectomy, potentially reducing pain and opioid use.
How similar studies have gone: Other studies have shown promising results with similar approaches in enhancing recovery after surgical procedures, suggesting potential for success in this trial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. American Society of Anesthesiologists (ASA) physical status II- III 2. BMI 35- 50 kg/m2 Exclusion Criteria: 1. Significant hepatic, renal, neuromuscular, or cardiac impairments 2. Extreme obesity (BMI \> 50 kg/m2) 3. Patients on current opioid medication 4. Allergies to dexmedetomidine or bupivacaine
Where it's running
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Alexandria Main University Hospital
Alexandria, Egypt Recruiting
Study contacts
- Study coordinator: Mai A El-Sayed, Lecturer of Anesthesia
- Email: m_mohamed165@alexmed.edu.eg
- Phone: 00201287459922
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Comparing two ultrasound-guided abdominal wall nerve blocks for pain after sleeve gastrectomy
This trial will test whether the external oblique intercostal plane (EOIP) block or the subcostal transversus abdominis plane (TAP) block gives better pain relief and lowers opioid use for adults having laparoscopic sleeve gastrectomy.
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Pain management technique for patients undergoing laparoscopic sleeve gastrectomy
This study is testing a new pain management technique to see if it can help people recovering from laparoscopic sleeve gastrectomy feel less pain and use fewer opioids after surgery.
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Comparing robotic and laparoscopic sleeve gastrectomy for obesity treatment
This study is testing whether robotic sleeve gastrectomy works better than laparoscopic sleeve gastrectomy for people with obesity in terms of pain, recovery, and quality of life after surgery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.