Laparoscopic Sleeve Gastrectomy

5

Review clinical trials related to Laparoscopic Sleeve Gastrectomy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Eating Behavior, Nutritional Status and Appetite Hormones After Bariatric Surgery

This study aims to evaluate changes in eating behavior attitudes, nutritional status, and appetite-regulating hormonal parameters in individuals who have undergone Laparoscopic Sleeve Gastrectomy (LSG). The study will be conducted at Bursa Yıldırım Doruk Hospital, Department of General Surgery. A total of 40 volunteer participants who underwent LSG within the last month will be included. Participants will be assessed at baseline (shortly after surgery) and at 6-month follow-up. Assessments will include anthropometric measurements (body weight, height, waist and hip circumference, BMI, waist-to-hip ratio), 3-day dietary intake records analyzed using BeBIS 8.2 software, and the Adult Eating Behavior Scale. Biochemical parameters including fasting blood glucose, total cholesterol, triglycerides, HDL, LDL, VLDL cholesterol, and insulin will be obtained from patient files and analyzed using Advia Chemistry 2400 and Advia XPT devices. Additionally, appetite-regulating hormones (ghrelin, GLP-1, PYY) will be analyzed from residual blood samples using the ELISA method with RelAssay Diagnostics kits by Teknogen Bioengineering Laboratory. All data will be compared between baseline and 6-month follow-up to evaluate the impact of bariatric surgery on nutritional and hormonal outcomes.

Participants needed: 40
Trial details
Age: 18-50Biological sex: AllType: ObservationalSponsor: Özlem ÖZPAK AKKUŞUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Having undergone Laparoscopic Sleeve Gastrectomy (LSG) within the last month [+6]

Not having undergone Laparoscopic Sleeve Gastrectomy (LSG) or not planning to un... [+6]

Status: Recruiting

Ultrasound-Guided External Oblique Intercostal Plane Block Versus Subcostal Transversus Abdominis Plane Block For Perioperative Analgesia in Laparoscopic Sleeve Gastrectomy

This study aims to compare the analgesic efficacy, duration of analgesia, and overall opioid consumption between the external oblique intercostal plane (EOIP) block and subcostal transversus abdominis plane (TAP) block in patients undergoing laparoscopic sleeve gastrectomy.

Participants needed: 70
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Benha UniversityUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Age from 18 to 65 years. [+5]

Patient refusal. [+6]

Status: Recruiting

Modified Thoracoabdominal Nerve Plane Block In Laparoscopic Sleeve Gastrectomy

Ultrasound-guided Modified Thoracoabdominal Nerve Plane Block (M-TAPA) is performed into the costochondral aspect at the 9th-10th costal level by injecting local anesthetics deep into the chondrium. It provides blockage of both the anterior and lateral cutaneous branches of the thoracoabdominal nerve. Studies show that M-TAPA block is effective for postoperative analgesia and other abdominal surgeries, but its effect on patients undergoing LSG surgery has not yet been studied. The hypothesis is that the M-TAPA block performed in patients undergoing Laparoscopic Sleeve Gastrectomy (LSG) Operation would reduce opioid consumption in the first 24 hours period after surgery.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Istanbul Medipol University HospitalUpdated: Dec 24, 2025Locations: 1
Eligibility criteria

with a history of bleeding diathesis, [+7]

Status: Recruiting

Effects of Assisted Robotic vs Laparoscopic Sleeve Gastrectomy

This will be a prospective, obesity-registry based, single-blind randomized controlled trial with a 1:1 allocation ratio. Specific inclusion criteria are all patients eligible to undergo a Laparoscopic sleeve gastrectomy (LSG) based on the current National Institute of Health (NIH) patient selection guidelines. Patients should be able to give consent, be deemed medically-cleared to undergo elective surgery, and tolerate general anesthesia. All enrollments and surgeries in this study will take place at the Cleveland Clinic Bariatric and Metabolic Institute. The study will consist of 2 interventions: laparoscopic sleeve gastrectomy (LSG) or robotic sleeve gastrectomy (RSG). The primary objective is early postoperative pain, but also surgeon ergonomics and patient quality of life will be compared. Additional outcomes include 30-day perioperative results, minor and major morbidities, serious adverse events, resolution of medical comorbidities, and weight loss in percent of excess weight lost (%EWL) at one year.

Participants needed: 91
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Ricard CorcellesUpdated: Dec 10, 2025Locations: 1
Eligibility criteria

All patients eligible to undergo a SG based on the current National Institute of...

patients with previous bariatric surgeries, emergency surgeries, with chronic op...

Status: Recruiting

Quality of Recovery in Laparoscopic Sleeve Gastrectomy Using Dexmedetomidine Infusion Versus Laparoscopic TAP Block in Combination With Paragastric Neural Block

The goal of this clinical trial is to learn which is better, combining Dexmedetomidine infusion and paragastric neural block or combining laparoscopic TAP block and paragastric neural block to enhance recovery after laparoscopic sleeve gastrectomy. The main questions it aims to answer are: Will using paragastric neural block (PGNB) combined with dexmedetomidine infusion give better recovery or using PGNB combined with laparoscopic transversus abdominis plane (LTAP) block in patients undergoing laparoscopic sleeve gastrectomy. This will be assessed by: Recording how much opioids were consumed by the patients Hemodynamic stability of the enrolled patients Pain scores as given by the patient The quality of postoperative patient recovery How many patients encountered nausea or vomiting

Participants needed: 60
Trial details
Phase: Phase 2, Phase 3Age: 20-60Biological sex: AllType: InterventionalSponsor: Alexandria UniversityUpdated: May 14, 2025Locations: 1
Eligibility criteria

American Society of Anesthesiologists (ASA) physical status II- III [+1]

Significant hepatic, renal, neuromuscular, or cardiac impairments [+3]