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Exendin-(9-39) for Post-Bariatric Surgery Glucose Metabolism (GLP-1 Trial)

Phase < 1
Recruiting
Led By Marzieh Salehi, MD,MS
Research Sponsored by The University of Texas Health Science Center at San Antonio
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
healthy control without diabetes or active organ disease
age 18-65
Must not have
GI obstruction
significant anemia
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

This trial is studying how well gastric bypass surgery works in improving glucose metabolism by looking at the mechanisms by which it does so.

Who is the study for?
This trial is for adults aged 18-65 who have had gastric bypass surgery and are experiencing recurrent low blood sugar. Healthy individuals without diabetes or active organ disease can also participate. People with significant anemia, current diabetes (unless awaiting bariatric surgery), pregnancy, or GI obstruction cannot join.
What is being tested?
The study aims to understand how gastric bypass improves blood sugar control by focusing on incretin hormones that affect insulin secretion. Participants will undergo tests like the intravenous-oral hyperglycemic clamp to investigate these effects.
What are the potential side effects?
Potential side effects from the interventions (exendin-(9-39)) may include reactions at the injection site, changes in blood sugar levels, nausea, and possible allergic reactions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I do not have diabetes or any active organ disease.
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I am between 18 and 65 years old.
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I have had weight loss surgery.
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I have had low blood sugar episodes after gastric bypass surgery.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have a blockage in my digestive tract.
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I have severe anemia.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: hyperglycemic clamp-Meal tolerance testExperimental Treatment1 Intervention
these studies are to evaluate the effect of exendin-9 on insulin secretion before and after meal ingestion in patients after bariatric surgeries compared to non-surgical controls
Group II: Labeled meal tolerance testExperimental Treatment1 Intervention
The effect of GLP-1 receptor blockade on glucose tolerance and glucose kinetics are evaluated in the group patients with bariatric surgery vs. nonsurgical using exendin-9-39 infusion during one of the the 2-day dual tracer studies of meal tolerance test

Find a Location

Who is running the clinical trial?

The University of Texas Health Science Center at San AntonioLead Sponsor
475 Previous Clinical Trials
92,236 Total Patients Enrolled
Marzieh Salehi, MD,MSPrincipal InvestigatorMarzieh Salehi

Media Library

exendin -(9-39) Clinical Trial Eligibility Overview. Trial Name: NCT01803451 — Phase < 1
Post-Bariatric Surgery Research Study Groups: hyperglycemic clamp-Meal tolerance test, Labeled meal tolerance test
Post-Bariatric Surgery Clinical Trial 2023: exendin -(9-39) Highlights & Side Effects. Trial Name: NCT01803451 — Phase < 1
exendin -(9-39) 2023 Treatment Timeline for Medical Study. Trial Name: NCT01803451 — Phase < 1
~3 spots leftby Aug 2025