| Trial ID: | L4628 |
| Source ID: | NCT00241423
|
| Associated Drug: |
Exenatide
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| Title: |
Effect of Exenatide on 24-Hour Blood Glucose Profile Compared With Placebo in Patients With Type 2 Diabetes
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| Acronym: |
|
| Status: |
COMPLETED
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| Study Results: |
NO
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| Results: |
|
| Conditions: |
Type 2 Diabetes Mellitus
|
| Interventions: |
DRUG: exenatide|DRUG: Placebo
|
| Outcome Measures: |
Primary: Time-averaged serum glucose during a 24-hour period, Time-averaged serum glucose during a 24-hour period, Every half-hour to hour for 24 hours | Secondary: To compare the effects of exenatide and placebo on serum glucose, To compare the effects of exenatide and placebo on serum glucose measured as averaged daytime glucose, averaged nighttime glucose, time-averaged postprandial glucose 2 hours after each meal, time-averaged postprandial glucose 4 hours after each meal, 2-hour postprandial glucose averaged across morning and evening meals, and averaged across the three meals, and fluctuation evaluations, Each half-hour to 2 hours for 24 hours
|
| Sponsor/Collaborators: |
Sponsor: AstraZeneca | Collaborators: Eli Lilly and Company
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| Gender: |
ALL
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| Age: |
ADULT, OLDER_ADULT
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| Phases: |
PHASE2
|
| Enrollment: |
30
|
| Study Type: |
INTERVENTIONAL
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| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
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| Start Date: |
2005-10
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| Completion Date: |
2007-06
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| Results First Posted: |
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| Last Update Posted: |
2015-02-23
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| Locations: |
Research Site, Washington, District of Columbia, United States|Research Site, San Antonio, Texas, United States
|
| URL: |
https://clinicaltrials.gov/show/NCT00241423
|