Non-Insulin-Dependent Diabetes Mellitus Clinical Trial
Official title:
An Exploratory MRI Study in Type 2 Diabetic Subjects: A Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Measurement of Fluid Volumes by MRI in the Lower Extremities of Subjects Receiving Pioglitazone
| Verified date | October 2008 |
| Source | GlaxoSmithKline |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Interventional |
This study will use Magnetic Resonance Imaging (MRI) techniques to evaluate changes in fluid volume in the lower legs of diabetic patients who add either pioglitazone or placebo to their current diabetic regimen.
| Status | Completed |
| Enrollment | 32 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 70 Years |
| Eligibility |
Inclusion criteria: - Must have been diagnosed with Type 2 diabetes at least three months prior to screening. - Must be taking either metformin and a sulfonylurea, metformin and insulin, or insulin only, and doses of these medications must have been stable for at least three months. - Must have a Body Mass Index (BMI) of between 24 and 35. - If female, the subject must be post-menopausal. - HbA1c levels must be between 7% and 10%. - Subjects must be eligible for MRI scanning (ie, no metal implants, pacemaker, etc). Exclusion criteria: - Suffer from claustrophobia. - Use of tobacco, nicotine, or illegal drugs of abuse. - Use of caffeine within two days prior to each study visit. - HIV, hepatitis, edema, untreated blood pressure problems, heart, lung, nervous system or kidney disease, history of blood clots in the legs, diabetic neuropathy, or untreated thyroid disease. - Use of drugs or medications that affect the levels of fluid in the body, such as diuretics. |
Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | GSK Investigational Site | Belmont | Massachusetts |
| Lead Sponsor | Collaborator |
|---|---|
| GlaxoSmithKline |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Changes in interstitial fluid volume in the lower extremities as measured by MRI. | |||
| Secondary | Assessments of other indicators of fluid volume changes, including labwork evaluation, fluid compartment volume measurement, direct measurement of the calf. |
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