Comparison Between Gastric Band, Laparoscopic Sleeve Gastrectomy, Gastric Bypass Surgeries

Outcomes Comparison Between Gastric Band, Laparoscopic Sleeve Gastrectomy, and Gastric Bypass Surgeries in Obese Adolescents

Determine the short and long term safety and efficacy of the Gastric bypass , laparoscopic sleeve gastrectomy, and Gastric banding (LAGB) on severely obese adolescents. The procedure selection is made by the patient or patient and guardian. This is not a randomized trial.

Study Overview

• Status: Active, not recruiting
• Conditions: Obese Adolescents

Detailed Description

Twenty-six obese adolescents with plans to undergo bariatric surgery for clinical treatment will be recruited for research study during screening process at the Yale Adolescent Bariatric Surgery Clinic. After the appropriate discussion with surgeon, the choice of procedure will be made by subject and legal guardian.

Every bariatric patient must have completed the thorough six-month evaluation period established by the Yale's Adolescent Bariatric Clinic.

This standard of care pre-operative testing provides as a screening tool to ensure every adolescent bariatric patient is mentally and physically appropriate for this surgery.

• Monthly visits with clinician (Pediatric Obesity/Diabetology Expert) and dietician to discuss lifestyle change management and anthropometric measures.
• Psychiatrist or psychologist to screen for depression, uncontrollable psychosis, suicidal ideation, and hostile or unsupportive family environment.
• Bone age will be obtained to ensure subject has reached or near full growth potential.
• Pediatric Cardiology for echocardiogram to rule out left ventricular hypertrophy.
• Oral glucose tolerance test to assess glucose status and degree of insulin resistance.
• Blood work to assess hepatic and kidney function, nutritional deficiencies, hormonal profile, and hyperlipidemia.
• Pediatric Pulmonary for sleep study and Pulmonary Function Tests (PFTs) to rule out obstructive sleep apnea.

When a subject is approved for surgery, he or she will meet with Bariatric Surgeon to discuss benefits and risks of each bariatric surgery. After the appropriate discussion with surgeon, the choice of procedure will be made by subject and legal guardian. For research purposes, we seek to monitor the progress of the patients enrolled in Yale's Adolescent Bariatric Surgery Clinic. Collecting pre and post long term operative data will allow us to describe this efficacy and potential complications that arise with RYGB vs LAGB.

As standard of care, all subjects will have undergone pre-operative testing established by Adolescent Bariatric Surgery Clinic before any of the bariatric surgeries.

For research purposes:

1. Month prior to Surgery

   • Oral Glucose Tolerance Test (OGTT)
   • Abdominal MRI (weight must not exceed 140 kg)
   • DNA blood extraction

   During RYGB or LAGB Surgery

   • Liver Biopsy
   • Visceral (omental fat) and Subcutaneous Fat Biopsy

   Data collection will continue for 24 months post-operatively and include both research testing and standard of care clinical appointments.

   Post Surgery 2 week 2 months 3 months 6 months 12 months 24 months Standard Of Care Post-op Post-op Post-op Post-op Post-op Post-op Anthropometric X X X X X X Measures Hemoglobin A1c X X X X X

2. Week 2 Month 3 Month 6 Month 12 Month 24 Month Post Surgery (research) Post-op Post-op Post-op Post-op Post-op Post-op OGTT X X X Abdominal MRI X X X X X X

Anthropometric Measures and HBA1c Anthropometric measures will be done at study enrollment, monthly leading up to the surgery RYGB or LAGB, and 2 weeks, 2 months, 3 months, 6 months, 12 months and 24 months post operatively. These measures include height, weight, BMI, BMI Z score, systolic and diastolic blood pressure, resting heart rate, % fat mass, and total fat mass. Demographic data includes ethnicity and family income. HbA1c will be completed at the 3, 6 , 12, and 24 month post operative time period.

• Study Type: Observational
• Enrollment (Actual): 26

Contacts and Locations

Study Locations

• United States
  • Connecticut
    • New Haven, Connecticut, United States, 06520
      • Yale Pediatric Endocrinology Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 19 years (Child, Adult)
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

The research subjects will be recruited from the Yale Pediatric Obesity Clinic and the Endocrine Clinic.

Description

Inclusion Criteria:

Youth 14-19yrs

• 6 months of attempts at weight management by primary care physician or Pediatric Endocrinologist
• Approval by the Adolescent Bariatric Surgery clinic to undergo surgery
• Physically or nearly physically mature
• BMI >= 35kg/m2 with one obesity related comorbidities or BMI >= 40 kg/m2
• Commitment to avoid pregnancy for at least 1 year postoperatively
• Capability and willingness to adhere to nutritional guidelines postoperatively
• Informed consent to surgical treatment
• Demonstration of decisional capacity
• Supportive family environment

Exclusion Criteria:

• Inability to be approved by Yale Adolescent Bariatric Surgery clinic to undergo surgery
• Uncontrolled psychosis
• Uncontrolled depression
• Drug or alcohol abuse
• History of congenital or acquired anomalies of gastrointestinal tract
• Esophageal anatomical abnormality or dysmotility
• Inflammatory bowel disease
• Severe cardiopulmonary disease
• Severe coagulopathy
• Hepatic insufficiency or cirrhosis
• Presence of localized or systemic infection at time of surgery
• Obesity related to central causes: Prader Willi and hypothalamic abnormalities
• Non-compliance to nutrition plan, exercise, and behavioral counseling/treatment
• Pregnant, breast-feeding or planning of becoming pregnant within 1-2 years of surgery

Study Plan

How is the study designed?

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort
Gastric Banding; Patients chose Gastric banding
Gastric Bypass; Patients chose gastric bypass surgical operation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Glucose Tolerance	Glucose tolerance changes measured by 3 hour oral glucose tolerance test.	baseline, 2 month, 3 month, 12 month

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Anthropometric data	Height, weight, body fat percentage changes	Baseline, 2 weeks, 2 mnths, 3 months, 6 months, 12 months, 24 months
Changes in nutritional health	Changes in vitamin/mineral blood levels	Baseline, 2 weeks, 2 mnths, 3 months, 6 months, 12 months, 24 months

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Fat distribution	Abdominal MRI	baseline, 2 weeks, 2 months, 3 months, 6 months, 12 months, 24 months

Collaborators and Investigators

• Sponsor: Yale University
• Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
• Investigators: Principal Investigator: Sonia Caprio, MD, Yale University

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2012
• Primary Completion (Estimated): August 1, 2026
• Study Completion (Estimated): December 1, 2026

Study Registration Dates

• First Submitted: November 11, 2013
• First Submitted That Met QC Criteria: December 4, 2013
• First Posted (Estimated): December 9, 2013

Study Record Updates

• Last Update Posted (Estimated): September 16, 2025
• Last Update Submitted That Met QC Criteria: September 9, 2025
• Last Verified: September 1, 2025

More Information

Terms related to this study

• Keywords: diabetes; pediatric obesity; bariatric_surgery
• Additional Relevant MeSH Terms: Endocrine System Diseases; Nutrition Disorders; Metabolic Diseases; Overnutrition; Body Weight; Glucose Metabolism Disorders; Overweight; Obesity; Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Signs and Symptoms; Diabetes Mellitus; Pediatric Obesity
• Other Study ID Numbers: 1109009034; 2R01HD028016-20A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO