Impact of Exenatide on Sleep Duration



Status:Completed
Conditions:Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 75
Updated:4/2/2016
Start Date:February 2011
End Date:June 2015
Contact:Annette Miller, MSN
Email:amiller@medicine.bsd.uchicago.edu
Phone:773-834-8871

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Impact of Exenatide on Sleep Duration and Quality in Type 2 Diabetes

This study investigates the effect of exenatide, a FDA approved medication for the treatment
of type 2 diabetes on sleep duration and quality. Individuals with type 2 diabetes will be
studied before and during treatment with Exenatide.

Enrolled individuals will be asked to come to the University of Chicago for 3-4 outpatient
visits over the course of 3-4 months.


Inclusion Criteria:

Patients taking diabetes medications other then insulin will be included, but changes to
their medications may be made as deemed necessary by their physician. Patients on stable
medications for chronic and co-morbid conditions (high blood pressure, high cholesterol,
etc) will be eligible

Exclusion Criteria:

Patients with moderate or severe kidney disease and history of pancreatitis or patients on
insulin will be excluded, as Exenatide use is contraindicated or risky in these
conditions.

Patients with unstable cardiac, neurological or psychiatric disease and women who are
pregnant or trying to get pregnant will be excluded. Patients who have severe COPD, severe
neuropathy or chronic pain, which could impair sleep, will be excluded. Shift workers will
be also excluded.
We found this trial at
2
sites
5801 South Ellis Avenue
Chicago, Illinois 60637
 773.702.1234
University of Chicago One of the world's premier academic and research institutions, the University of...
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Chicago, IL
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5801 South Ellis Avenue
Chicago, Illinois 60637
 773.702.1234
University of Chicago One of the world's premier academic and research institutions, the University of...
?
mi
from
Chicago, IL
Click here to add this to my saved trials