Determinants of Diabetes Remission After Gastric Bypass Surgery
NCT ID: NCT02287285
Last Updated: 2020-04-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
EARLY_PHASE1
25 participants
INTERVENTIONAL
2014-10-31
2019-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Contribution of Incretin Hormones to the Amelioration of Glucose Metabolism After Roux-en-Y Gastric Bypass
NCT01843855
Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass
NCT01803451
To Define the Role of GLP-1 for Improving Glucose Homeostasis in Humans Following Gastric Bypass Surgery
NCT02204813
Role of GLP-1 in Hyperinsulinemic Hypoglycemia Post-bariatric Surgery
NCT02550145
The Importance of GLP-1 in Post RYGB Improvement in Glycaemic Control Type 2 Diabetic Subjects
NCT01579981
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exendin9
Longitudinal study of insulin secretion and sensitivity in patients with type 2 diabetes before and after gastric bypass surgery.
Exendin9
Dosed at 600 pmol/kg/min for 210 minutes.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exendin9
Dosed at 600 pmol/kg/min for 210 minutes.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Blood pressure is under at least moderate control \<160/100 mmHg
* Patients can be on dyslipidemia medications but need fasting triglyceride \< 600 mg/dl
* Patients without recent (last 6 months) history of cardiovascular disease (CVD)
* BMI \> 35 and \< 55 kg/m2 prior to GBP surgery
Exclusion Criteria
* Unstable angina
* Recent stroke
* Current therapy that may affect glucose metabolism such as glucocorticoids, HIV medications, etc
* Active infection
* Kidney failure
* Severe liver dysfunction
* Severe respiratory or cardiac failure
* History of allergic reaction to exendin 9-39
* History of pancreatitis, history of cholelithiasis, history of alcoholism
* Presence of high triglyceride levels (\>600 ng/dl)
* Pregnancy (a pregnancy test will be done prior to enrollment and prior to each procedure in all premenopausal women)
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institutes of Health (NIH)
NIH
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
Blandine Laferrere
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Blandine Laferrere
Professor of Medicine, Columbia University
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Blandine Laferrere, MD
Role: PRINCIPAL_INVESTIGATOR
New York Obesity Nutrition Research Center, Columbia University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
New York Obesity Research Center, Columbia University
New York, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Prasad M, Mark V, Ligon C, Dutia R, Nair N, Shah A, Laferrere B. Role of the Gut in the Temporal Changes of beta-Cell Function After Gastric Bypass in Individuals With and Without Diabetes Remission. Diabetes Care. 2022 Feb 1;45(2):469-476. doi: 10.2337/dc21-1270.
Shah A, Holter MM, Rimawi F, Mark V, Dutia R, McGinty J, Levin B, Laferrere B. Insulin Clearance After Oral and Intravenous Glucose Following Gastric Bypass and Gastric Banding Weight Loss. Diabetes Care. 2019 Feb;42(2):311-317. doi: 10.2337/dc18-1036. Epub 2018 Dec 6.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.