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| Sponsor: | Taichung Veterans General Hospital |
|---|---|
| Collaborator: |
Tri-Service General Hospital |
| Information provided by: | Taichung Veterans General Hospital |
| ClinicalTrials.gov Identifier: | NCT00417950 |
Purpose
To understand if acarbose, an alpha-glucosidase inhibitor usually for treating diabetes, will further lower post meal glucose and inflammatory state when taking together with moderate amount of alcohol during meal tolerance test in subjects with impaired glucose tolerance or mild diabetes.
| Condition | Intervention |
|---|---|
|
Diabetes Mellitus Impaired Glucose Tolerance |
Drug: Acarbose |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
Eligibility| Ages Eligible for Study: | 25 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: I Te Lee, MD, MS | 886-4-23592525 ext 3065 | itlee@vghtc.gov.tw |
| Taiwan | |
| Taichung Veterans General Hospital | Recruiting |
| Taichung, Taiwan | |
| Contact: Wayne H Sheu, MD, PhD 886-4-23592525 ext 3068 whhsheu@vghtc.gov.tw | |
| Principal Investigator: Wayne H Sheu, MD, PhD | |
| Sub-Investigator: I Te Lee, MD, MS | |
| Principal Investigator: | Wayne H Sheu, MD, PhD | Taichung Veterans General Hospital |
More Information
| ClinicalTrials.gov Identifier: | NCT00417950 History of Changes |
| Other Study ID Numbers: | 950801/C06138 |
| Study First Received: | January 1, 2007 |
| Last Updated: | January 3, 2007 |
| Health Authority: | Taiwan: Department of Health |
|
diabetes acarbose alcohol |
inflammation oxidative stress Mild diabetes mellitus |
|
Diabetes Mellitus Glucose Intolerance Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Hyperglycemia |
Acarbose Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Hypoglycemic Agents Physiological Effects of Drugs |