Post-bariatric Surgery

3

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

Condition / disease
Location
Status: Recruiting

Concurrent Exercise Effects in Post-Bariatric Patients

This study aims to evaluate the effect of a 5-week concurrent exercise program (aerobic and resistance training) on muscle quality, body composition, functional response, and quality of life in individuals undergoing bariatric surgery. This is a single-center, prospective, longitudinal, randomized controlled clinical trial with two parallel groups: an intervention group and a control group. A total of 87 adults aged 18 to 60 years who have undergone sleeve gastrectomy or Roux-en-Y gastric bypass and have a medical indication for metabolic rehabilitation will be recruited. The intervention group will participate in a structured, semi-supervised concurrent exercise program for 5 weeks, consisting of two in-person sessions per week (10 sessions in total), whereas the control group will continue receiving usual kinesiology care and standard clinical management according to the institutional rehabilitation protocol at Clínica BUPA Santiago. All participants will be assessed at two time points: baseline, during the fourth postoperative week, and at week 7. The primary outcome will be the change in rectus femoris muscle quality assessed by ultrasound (echo intensity). Secondary outcomes will include body composition (bioelectrical impedance analysis), functional response (One-minute Sit-to-Stand Test), and quality of life (Moorehead-Ardelt II questionnaire). Additionally, adherence to the exercise program in the intervention group will be assessed as the percentage of attendance at supervised exercise sessions, and its association with the magnitude of changes in study outcomes will be explored. The findings are expected to provide clinically relevant evidence regarding the effectiveness of exercise during the early postoperative period and to contribute to the optimization of metabolic rehabilitation strategies following bariatric surgery.

Participants needed: 87
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Universidad Autónoma de ChileUpdated: Sep 25, 2026Locations: 1
Eligibility criteria

Adults aged 18-60 years. [+4]

Type 1 diabetes mellitus or type 2 diabetes mellitus with severe complications (... [+6]

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

Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass

The overall goal of this project is to understand the mechanisms by which gastric bypass surgery improves glucose metabolism. The central hypothesis guiding this project is that the reconfiguration of intestinal transit with the Roux-en-Y will increase the release of insulinotropic GI hormones, termed incretins that improve insulin secretion and glucose metabolism. The study is divided into three specific aims. 1. To determine the role of incretin hormones on insulin secretion in patients with gastric bypass surgery using intravenous-oral hyperglycemic clamp. 2. To compare incretin effect and glucose tolerance among patient who suffer from hypoglycemia after RYGB and asymptomatic surgical and non-surgical individuals. 3. To quantify the contribution of GLP-1 to incretin effect enhancement following surgery.

Participants needed: 80
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

age 18-65 [+3]

pregnancy [+3]