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Search / Trial NCT00992901

Role of Neural and Hormonal Regulation Factors on Insulin Secretion After Gastric Bypass Surgery

Launched by THE UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO · Oct 8, 2009

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Gastric Bypass Surgery Glucose Tolerance Insulin Response To Meal Ingestion Gut Hormone And Neural Response To Meal Ingestion

ClinConnect Summary

This clinical trial is studying how certain factors in the body affect insulin secretion in patients who have undergone Roux-en-Y gastric bypass (RYGB) surgery. RYGB is a type of weight loss surgery that has been found to improve blood sugar control in people with type 2 diabetes, even before they lose significant weight. However, some patients later experience dangerously low blood sugar levels, known as hypoglycemia. The researchers want to understand how hormones from the gut, particularly one called GLP-1, and changes in nerve activity might influence insulin production in these patients.

To participate in this trial, individuals must be between the ages of 65 and 74 and meet certain health conditions. Eligible participants include those who have experienced low blood sugar after RYGB surgery, asymptomatic individuals who have had bariatric surgery, and healthy people without a history of diabetes. Participants will need to visit the Cedars-Sinai Medical Center for evaluations. The study aims to gather important information about how RYGB affects insulin and could provide insights that help improve care for patients experiencing hypoglycemia after surgery.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Hypoglycemic RYGB patients with documented blood glucose level \<50 mg/dl
  • Asymptomatic individuals with bariatric surgery
  • Healthy non-surgical patients with no personal history of diabetes
  • Subjects must physically be able to come to our clinical research center at Cedars-Sinai Medical Center
  • Exclusion Criteria:
  • Active heart, lung, liver, gastrointestinal or kidney disease; unable to give informed consent; pregnancy; uncontrolled high blood pressure or high cholesterol; significant anemia (hemoglobin \<11g/dL); prisoners or institutionalized individuals; type 2 diabetes melitis; development of any serious medical or psychiatric illness during recruitment or studies;
  • RYGB patients will also be disqualified if they have gastric outlet obstruction or severe diarrhea
  • Healthy non-surgical patients with personal history of diabetes
  • For administration of atropine, the following exclusions also apply:
  • History of glaucoma
  • Uncontrolled hypertension (any subjects with BP\>140/90 and history of dyslipidemia
  • Taking any medication that might interact with atropine and cannot be stopped will be excluded from the study)
  • Myasthenia gravis
  • Brain pathology
  • Enlarged prostate in men

About The University Of Texas Health Science Center At San Antonio

The University of Texas Health Science Center at San Antonio (UT Health San Antonio) is a leading academic medical institution dedicated to advancing health through education, research, and patient care. As a prominent sponsor of clinical trials, UT Health San Antonio focuses on innovative medical research aimed at improving health outcomes across diverse populations. With a commitment to excellence, the institution fosters collaboration among its multidisciplinary teams to explore cutting-edge therapies and interventions. Through rigorous scientific inquiry and ethical practices, UT Health San Antonio strives to make meaningful contributions to the field of medicine and enhance the quality of life for patients.

Locations

San Antonio, Texas, United States

San Antonio, Texas, United States

Patients applied

0 patients applied

Trial Officials

Marzieh Salehi, MD, MS

Principal Investigator

Marzieh Salehi

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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