The Effects of Bariatric Surgeries on Glucose Metabolism
Launched by THE UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO · Jul 5, 2016
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating how two types of weight-loss surgeries, gastric bypass and sleeve gastrectomy, affect the way our bodies handle sugar after we eat. Researchers want to understand the changes in hormone and nerve signals that happen after these surgeries, especially focusing on patients who experience low blood sugar (hypoglycemia) after gastric bypass surgery.
If you're between the ages of 65 and 74, have had gastric bypass surgery and have had low blood sugar levels below 50 mg/dl, or if you’re a healthy person with no diabetes history, you may be eligible to participate. Participants will visit the Cedars-Sinai Medical Center for the study, where they will undergo tests and evaluations to help researchers gather important information. It’s important to note that individuals with certain health conditions, like active heart or kidney disease, or those who are pregnant, cannot participate. Overall, this study aims to improve understanding of how these surgeries affect blood sugar levels, which could lead to better care for patients in the future.
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 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 mellitis; development of any serious medical or psychiatric illness during recruitment or studies;
- • RYGB patients will 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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Antonio, Texas, United States
San Antonio, Texas, United States
Patients applied
Trial Officials
Marzieh Salehi, MD, MS
Principal Investigator
The University of Texas Health Science Center at San Antonio
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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