Sleeve Gastrectomy

16

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

Condition / disease
Location
Status: Not yet recruiting

Pilot Study of Salivary Bile Acids and Pepsin as Predictive Biomarkers of Reflux Disease After Sleeve Gastrectomy

The goal of this observational study is to learn whether bile acids and pepsin in saliva can help identify adults at higher risk of developing reflux-related esophageal disease after sleeve gastrectomy, including Los Angeles grade B-D erosive esophagitis and Barrett's esophagus. The study will include adults undergoing sleeve gastrectomy as part of their regular clinical care. Participants will be evaluated before and after surgery and will serve as their own comparison group over time. The main questions it aims to answer are: Are saliva bile acids and pepsin linked to Los Angeles grade B-D erosive esophagitis or Barrett's esophagus after sleeve gastrectomy? How do saliva bile acids and pepsin change before and after sleeve gastrectomy? Can saliva bile acids and pepsin become useful biomarkers for detecting reflux-related esophageal disease after sleeve gastrectomy? Are saliva biomarker levels linked to reflux symptoms and endoscopy results after surgery? Researchers will compare saliva biomarker levels before and after surgery and between participants with and without reflux-related esophageal disease. Participants will: Provide saliva samples before surgery and at 12 and 36 months after surgery Provide fasting and post-meal saliva samples Undergo routine postoperative clinical follow-up and upper gastrointestinal endoscopy Complete reflux symptom questionnaires during follow-up The study will also explore whether saliva biomarkers could help select participants for follow-up endoscopy after sleeve gastrectomy.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Hospital de MataróUpdated: May 26, 2026Duration: 3 Years
Eligibility criteria

Adults aged 18 years or older undergoing sleeve gastrectomy at a participating c... [+4]

According to Lyon 2.0 criteria, participants with previous evidence of conclusiv... [+6]

Status: Not yet recruiting

Intertransverse Process Block Versus External Oblique Intercostal Plane Block After Laparoscopic Sleeve Gastrectomy

This randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Intertransverse Process Block (ITPB) and the Subcostal External Oblique Intercostal Plane Block (EOIPB) in patients undergoing laparoscopic sleeve gastrectomy. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block-related complications and adverse effects (hematoma, pneumothorax, local anesthetic systemic complications, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, quality of recovery assessed using the QoR-15 questionnaire, and incidence of postoperative nausea and vomiting.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Antalya City HospitalUpdated: May 15, 2026
Eligibility criteria

Patients aged 18-65 years [+5]

Refusal to participate [+8]

Status: Not yet recruiting

Intertransverse Process Block Versus Subcostal Transversus Abdominis Plane Block After Laparoscopic Sleeve Gastrectomy

This randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Intertransverse Process Block (ITPB) and the Subcostal Transversus Abdominis Plane Block (TAPB) in patients undergoing laparoscopic sleeve gastrectomy. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block-related complications and adverse effects (hematoma, pneumothorax, local anesthetic systemic complications, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, quality of recovery assessed using the QoR-15 questionnaire, and incidence of postoperative nausea and vomiting.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Antalya City HospitalUpdated: May 15, 2026Locations: 1
Eligibility criteria

Patients aged 18-65 years [+5]

Refusal to participate [+8]

Status: Recruiting

Stanford Program to Accelerate Robotic Children's Surgery

The goal of this clinical trial is to provide additional data to confirm safety and performance of the da Vinci Xi Surgical System in a human clinical setting. This pilot study is intended to provide an initial assessment to evaluate the feasibility, safety, and effectiveness for the utilization of the da Vinci Xi on pediatric and adolescent patients. This clinical trial will be conducted under the auspices of Stanford University's IRB approval.

Participants needed: 250
Trial details
Age: 6-21Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Subject is between 6 - 21 years of age (weighing at least 15 kilograms) [+4]

Subject with uncorrected coagulopathy [+5]

Status: Not yet recruiting

Comparison of the Effects of External Oblique Intercostal Plane Block and Subcostal Transversus Plane Block Methods With Ultrasound Guidance on Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy Operations

The primary aim of this study was to investigate the effects of the external oblique intercostal plane block and the subcostal transversus abdominis plane block on postoperative pain scores and opioid consumption in patients undergoing laparoscopic sleeve gastrectomy.

Participants needed: 90
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Sanliurfa Education and Research HospitalUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Adult patients aged between 18 and 65 years [+1]

Patients younger than 18 years or older than 65 years [+4]

Status: Recruiting

Mechanistic and Clinical Outcomes of a Surgical Innovation Aimed at Minimizing GERD Associated With VSG (INNOVATE-VSG)

This is a two-site randomized clinical trial aiming to test whether a modified investigational bariatric surgical procedure can improve gastroesophageal reflux disease (GERD) after sleeve gastrectomy.

Participants needed: 44
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of California, IrvineUpdated: Apr 13, 2026Locations: 2
Eligibility criteria

Male and female subjects aged 18-65 years [+6]

Hiatal hernia >2cm (defined as maximum axial height from end of the esophagus to... [+19]

Status: Recruiting

Impact of Foot Reflexology on Nausea After Obesity Surgery

Obesity is a major public health issue. The Obépi epidemiological survey, the results of which were published in 2020, shows a steady increase in obesity among the French population. Currently, more than 23 million French people are overweight or obese, and more than 8 million French people are obese. The most effective treatment currently available is surgery. These procedures are governed by specific recommendations. Between 50,000 and 60,000 procedures are performed in France each year. Three procedures are authorised: gastric banding, sleeve gastrectomy and gastric bypass. Hallyday \& al report 65% of patients experiencing nausea/vomiting after bariatric surgery. In 2019, Suh \& al showed that nausea and vomiting were more common after sleeve gastrectomy and that they were responsible for an increase in the length of hospitalisation. These episodes of nausea and vomiting occur within 48 hours after sleeve gastrectomy and can cause difficulties in resuming eating. One of the factors contributing to the occurrence of nausea and vomiting was the use of opioids. The benefits of foot reflexology were reported in 2023 by Dr Carrazé in rectal surgery. His doctoral thesis in medicine showed that foot reflexology sessions on days 1, 2 and 3 following rectal surgery reduced post-operative ileus and post-operative pain. The reduction in post-operative ileus led to a decrease in episodes of nausea and vomiting. In 2021, Murat-Ringot \& al demonstrated the beneficial effect of foot reflexology on nausea and vomiting during chemotherapy sessions, in addition to the anti-emetic treatments used for prevention. Anderson \& al. in 2021 also demonstrated a beneficial effect on pain in cancer patients, with no effect on nausea. The principle of foot reflexology is based on the fact that each organ, gland or part of the body corresponds to a reflex zone on the foot, hand, ears or face. Stimulation of the reflex zones is thought to activate the autonomic nervous system. Currently, there is very little scientific evidence on how this practice works and what its effects are. Despite various scientific publications on the results of foot reflexology, scientific evidence of its effectiveness remains weak. Only one prospective randomised trial has been found in the literature (Dalal \& al.) on the quality of life of patients with epilepsy. Despite the lack of high-quality studies, it appears that foot reflexology could benefit patients by reducing nausea and vomiting. To date, no studies have evaluated its effectiveness in the post-operative period, particularly after bariatric surgery. The aim of our randomised trial is to evaluate the impact of foot reflexology on nausea and vomiting after sleeve gastrectomy.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Departemental VendeeUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Adult patient [+3]

Patients receiving long-term morphine and opioid treatment [+7]

Status: Recruiting

Post-sleeve Gastrectomy Gastroesophageal Reflux Disease Prediction

Researchers are trying to identify predictors for gastroesophageal reflux disease after sleeve gastrectomy.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Mar 5, 2026Locations: 2
Eligibility criteria

Adult patients > 18 years [+3]

Participants who have LA grade C or D esophagitis, Barrett mucosa or peptic stri... [+3]

Status: Recruiting

Iron Supplementation and Anemia After Sleeve Gastrectomy

The goal of this observational study is to learn if taking extra iron pills after weight loss surgery helps prevent low iron and anemia compared to just taking a standard multivitamin. The main question it aims to answer is: Does a specific iron supplementation plan lower the number of patients who develop iron deficiency anemia in the 6 months after sleeve gastrectomy surgery? Researchers will compare two groups of patients from different hospital units to see if the extra iron works: Patients from one unit who take a prophylactic iron supplement (Ferrodep, 60 mg per day) in addition to their standard multivitamin. Patients from another unit who take only a standard multivitamin (Centrum Silver). Participants in this study will: * Have their blood tested for iron and anemia levels before surgery, and again at 3 and 6 months after surgery, as part of their regular post-operative care. * Be asked about their health and quality of life during follow-up clinic visits. * Have their medical information from their hospital records reviewed by the study team to track their progress.

Participants needed: 66
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Feb 11, 2026Locations: 1Duration: 6 Months
Eligibility criteria

Adults aged 18 to 65 years scheduled to undergo primary laparoscopic sleeve gast... [+2]

Prior history of major gastrointestinal surgery (e.g., bowel resection, gastrect... [+3]

Status: Recruiting

Gastro-Intestinal Digestion and Physiology After Bariatric Surgery

The goal of this clinical trial is to characterize gastrointestinal digestion and physiology in patients after bariatric surgery, or people living with obesity. The main question it aims to answer is: what is the status of gastrointestinal digestion and physiology after bariatric surgery? Participants will have two study visits: 1) participants will undergo collection of gastrointestinal samples and 2) participants will ingest an ingestible capsule that measures multiple physiological parameters along the gastrointestinal tract.

Participants needed: 51
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Universitaire Ziekenhuizen KU LeuvenUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

Voluntary written informed consent of the participant has been obtained prior to... [+3]

Patient has history of more than one bariatric surgery [+18]

Status: Recruiting

Study of the Link Between MASH ( Metabolic Dysfunction-Associated Steatohepatitis) and MAMs (Mitochondria-Associated Membranes ) Alteration in Patients Undergoing Bariatric Surgery - MAMBA

The main research hypothesis is that alterations in the communication between the endoplasmic reticulum (ER) and the mitochondria at contact sites called mitochondria-associated membranes (MAMs) occurs in different hepatic cell types of patients with Metabolic Dysfunction-Associated Steatotic Liver Disease (MALSD) and is involved in the progression towards MASH and could also influence the process of improvement of MASH. This study aims to investigate the link between Metabolic Dysfunction-Associated Steatohepatitis (MASH) and Mitochondria-Associated Membranes (MAMs) in liver cells and peripheral blood mononuclear cells (PBMCs) in patients undergoing bariatric surgery. The primary objective is to analyze MAMs alterations in hepatocytes in MASH patients compared to non-MASH patients. Secondary objectives include evaluating the correlation between MAMs in PBMCs and liver cells and assessing MAMs changes post-bariatric surgery.

Participants needed: 20
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: Hospices Civils de LyonUpdated: Jan 15, 2026Locations: 2
Eligibility criteria

Female or male adult patients [+4]

Patient presenting Hepatitis B as defined as presence of hepatitis B surface ant... [+22]

Status: Recruiting

Powered Handle Primary Sleeve Gastrectomy Study

The objective of this prospective, single arm, single-center study is to evaluate patients who are undergoing primary sleeve gastrectomy procedures and are surgically treated with the AEON Endoscopic Powered Handle Stapler and Stapler Reload. The primary endpoint is to assess the percentage of patients who encountered post-operative staple line complications (bleeding or leak), defined as requiring blood transfusion or revision surgery due to staple line complications.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Lexington Medical Inc.Updated: Jan 14, 2026Locations: 1
Eligibility criteria

Be within the range of 18-65 years of age [+2]

Prior bariatric surgery procedure [+9]

Status: Recruiting

The Effects of Bariatric Surgeries on Glucose Metabolism

The purpose of this study is learn the effect of gastric bypass surgery and sleeve gastrectomy on glucose metabolism mediated by neural and hormonal factors initiated after eating.

Participants needed: 200
Trial details
Phase: Early Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center at San AntonioUpdated: Sep 9, 2025Locations: 2
Eligibility criteria

Hypoglycemic RYGB patients with documented blood glucose level <50 mg/dl [+3]

Active heart, lung, liver, gastrointestinal or kidney disease; unable to give in... [+8]

Status: Recruiting

Vestibular Function in Obesity

Previous studies have demonstrated that obesity negatively affects the human vestibular system. However, whether improvement in vestibular function occurs following the resolution of obesity remains an area requiring further investigation. Therefore, the investigators aimed to assess and analyze vestibular system functions in patients scheduled for bariatric surgery, both before the surgery, after the surgery, and following significant weight loss. Participants aged between 18 and 60 years who meet the inclusion criteria will be enrolled in the study. Initially, participants will undergo medical history assessment and Body Mass Index (BMI) measurement. The enrolled participants will be evaluated using the following tests at three different time points-preoperatively, at the 1st month postoperatively, and at the 6th month postoperatively: Video Head Impulse Test (vHIT), static posturography test, Berg Balance Scale, SF-12 Quality of Life Scale, and the Activity-specific Balance Confidence (ABC) Scale. Although obesity has been shown to be associated with impaired postural balance, studies evaluating the direct effect of BMI on postural sway are limited. The aim of our study is to assess the vestibular system in obese patients before and after bariatric surgery. Through this, the investigators hope to contribute to the literature by providing balance assessments in individuals with obesity

Participants needed: 30
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Istanbul Aydın UniversityUpdated: Jun 24, 2025Locations: 1
Eligibility criteria

The native language must be Turkish [+4]

Status: Recruiting

Alcohol After Bariatric Surgery 2

The goal of this observational study is to learn how the body processes ingested alcohol and how alcohol affects mood and blood sugar in both men and women after undergoing sleeve gastrectomy. The main question\[s\]it aims to answer are: * Are there differences in the way that ingested alcohol is handled in men versus women after sleeve gastrectomy? * What is the consequence of drinking alcohol on an empty stomach versus after a meal on blood sugar control after undergoing sleeve gastrectomy? Participants will participate in two types of alcohol tests (alcohol given orally or administered intravenously) after not eating anything overnight or after having a meal. Researchers will compare men and women who underwent sleeve gastrectomy with men and women who had no surgery, are of similar age and body composition, and have similar alcohol intake patterns.

Participants needed: 88
Trial details
Age: 21-64Biological sex: AllType: ObservationalSponsor: University of Illinois at Urbana-ChampaignUpdated: Mar 11, 2025Locations: 1
Eligibility criteria

Male and female, 21-64 yrs. of age [+4]

For all groups (surgery and non-surgery groups) [+9]

Status: Not yet recruiting

Morbid Obesity and Severe Knee Osteoarthritis - Which Should Be Treated First?

The goal of this study is to determine whether undergoing bariatric surgery before knee replacement leads to better outcomes compared to undergoing knee replacement before bariatric surgery. Our secondary goal is to compare complication rates between these groups to determine if there is a difference based on the order of the two procedures. Participants will be randomly placed in one of two groups, with each undergoing both procedures but in opposite order. Quality of life will be assessed via questionnaires before and between each procedure, and rates of complications will also be documented to compare their rates between groups.

Participants needed: 142
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Memorial University of NewfoundlandUpdated: Jan 30, 2025Locations: 2
Eligibility criteria

BMI > or = 35, on surgical waitlist for a total knee arthroplasty and laparoscop...

a history of revision surgery, surgery for neoplastic disease, significant menta...