Post Bariatric Hypoglycemia

4

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

Condition / disease
Location
Status: Recruiting

Comparison of Hormonal Response to a Mixed-Meal Tolerance Test After Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic Sleeve Gastrectomy With Duodenojejunal Bypass in Patients With Super Morbid Obesity

Obesity is a major global health problem. Bariatric surgery is the most effective treatment, leading to substantial weight loss and improvement in obesity-related comorbidities. The most commonly performed procedures are Laparoscopic Roux-en-Y gastric bypass (LRYGB) and Laparoscopic sleeve gastrectomy (LSG). LRYGB is typically selected for patients with a BMI exceeding 50 kg/m2. Recently, LSG with duodenojejunal bypass (LSG-DJB) has been introduced. To date, no randomized controlled trial has compared LRYGB and LSG-DJB in patients with super morbid obesity, particularly regarding postoperative hormonal responses. This study aims to address this gap. If LSG-DJB results in a lower incidence of post-bariatric hypoglycemia than LRYGB, it would support its clinical benefit. Evaluation of GLP-1, GIP, glucagon, and insulin responses will clarify mechanisms underlying weight loss and postprandial glycemic changes.

Participants needed: 32
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Chulalongkorn UniversityUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Patients with an indication for bariatric surgery [+2]

Patients with diabetes mellitus [+6]

Status: Available

An Expanded Access Protocol to Provide Avexitide in Patients With Post-Bariatric Hypoglycemia

The Expanded Access Program will provide access to avexitide for people with post-bariatric hypoglycemia (PBH) following Roux-en-Y gastric bypass (RYGB) who meet the eligibility criteria for this program. The safety of avexitide and patient treatment experience will be monitored during this program.

Trial details
Age: 18+Biological sex: AllType: Expanded AccessSponsor: Amylyx Pharmaceuticals Inc.Updated: Jul 14, 2026Locations: 4
Eligibility criteria

Category A: Individuals who have completed the LUCIDITY trial through the Week 4... [+9]

Use of GLP-1 receptor agonists, glucose-dependent insulinotropic polypeptide (GI... [+8]

Status: Recruiting

Continuous Glucose Monitoring With iCan i3 in Post-Bariatric Patients With Late Dumping Syndrome

Late dumping syndrome is a common complication following Roux-en-Y gastric bypass, characterized by postprandial hypoglycemia with significant impact on patient safety and quality of life. Traditional capillary glucose monitoring has limited ability to detect rapid glycemic fluctuations. This prospective randomized study aims to evaluate the efficacy and safety of the iCan i3 continuous glucose monitoring (CGM) system compared to conventional capillary glucose monitoring in detecting hypoglycemic events in post-bariatric patients with late dumping syndrome. Participants will be randomized into two groups: one using CGM and one using standard fingerstick monitoring, and followed for 60 days. Clinical outcomes, hypoglycemia frequency, symptom correlation, and quality of life will be assessed.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Kaiser Clinic and HospitalUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Age 18-65 years [+4]

Diagnosis of diabetes mellitus under treatment [+7]

Status: Recruiting

Role of Nutrient Transit in Hyperinsulinemic Hypoglycemia

Severe hypoglycemia (low blood sugar)after gastric bypass surgery is an increasingly recognized condition, characterized by symptoms of hypoglycemia after eating and inappropriately elevated insulin concentrations that occur at the time of hypoglycemia. Severe hypoglycemia can be dangerous and debilitating and can also impact cognitive function. At the moment no medical therapies have been developed for this disorder. Determining why some but not other patients develop this condition would allow for improved prediction, prevention, and treatment approaches. The purpose of the study is to understand the physiological changes observed in those patients who undergo gastric bypass and develop symptomatic hypoglycemia.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Dec 4, 2024Locations: 1
Eligibility criteria

Male or female patients 18-70 years of age [+2]

Patients currently using sulfonylureas or other medications that may interfere w... [+7]