Trial ID: | L3608 |
Source ID: | NCT04321395
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Associated Drug: |
Vigabatrin
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Title: |
Vigabatrin and Insulin Sensitivity
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Acronym: |
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Status: |
COMPLETED
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Study Results: |
YES
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Results: |
https://ClinicalTrials.gov/show/NCT04321395/results
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Conditions: |
NAFLD|Obesity
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Interventions: |
DRUG: Vigabatrin
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Outcome Measures: |
Primary: Insulin Sensitivity, Measured by hyperglycemic euglycemic clamp, 3 weeks after initiation of treatment | Secondary: Oral Glucose Tolerance, Measured by 75 gram oral glucose tolerance test, 3 weeks after initiation of treatment|Oral Glucose Insulin Sensitivity, Insulin sensitivity based on oral glucose tolerance. Values are calculated using glucose and insulin from a 3-hour 75 gram oral glucose tolerance test at 0, 2, and 3 hours. Higher values are indicate better insulin sensitivity., After 3 weeks on drug
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Sponsor/Collaborators: |
Sponsor: Washington University School of Medicine
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Gender: |
ALL
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Age: |
ADULT
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Phases: |
PHASE2
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Enrollment: |
4
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: OTHER
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Start Date: |
2021-08-23
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Completion Date: |
2024-05-15
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Results First Posted: |
2025-01-14
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Last Update Posted: |
2025-01-14
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Locations: |
Washington University in St. Louis, Saint Louis, Missouri, 63110, United States
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URL: |
https://clinicaltrials.gov/show/NCT04321395
|