The purpose of this study is to determine whether exenatide and pramlintide will improve
blood glucose control after meals when compared to insulin alone.
Drug: Insulin and Exenatide
Drug: Insulin and Pramlintide
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Locations near you
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Full eligibility criteria for NCT00923715
Ages eligible for Study
12 Years to 21 Years
Genders eligible for Study
Accepts Healthy Volunteers
Age of 12 to 21 years.
HbA1C less than 9%
Subjects must be on intensive insulin management
C-peptide less than 0.3 ng/ml
Tanner stage greater than or equal to 3
Having T1DM for at least one year
T1DM defined by ADA criteria and having at least one of the following antibodies a. Anti-GAD (glutamic acid decarboxylase) b. Anti-islet cell 512 (ICA512) c. Anti-insulin
Willing to give consent.
Type 2 diabetes.
Having any other chronic condition except hypothyroidism stable on medications.
On chronic medications that may affect glucose excursions.
Anemia as defined as Hb less than 9 gm/dl.
Abnormal AST, ALT, amylase, lipase or creatinine (twice normal).
Unsupportive family environment as determined by clinicians and/or social workers.
Pregnant or lactating mothers
All locations for NCT00923715
United States (1)
Montefiore Medical Center CRC
Bronx, New York, United States, 10461
View full eligibility
Tris trial is registered with FDA with number: NCT00923715. The sponsor of the trial is Baylor College of Medicine and it is looking for 63 volunteers for the current phase.
Official trial title: Exenatide (Byetta) Vs Pramlintide (Symlin): Role in Post-Prandial Hyperglycemia
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