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Completed Phase 3 Interventional

Rosiglitazone on Microalbuminuria in Type 2 Diabetics

ClinicalTrials.gov ID: NCT00500955

Public ClinicalTrials.gov record NCT00500955. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 2, 2026, 2:45 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study to Evaluate the Efficacy of Rosiglitazone (BRL-049653) on Reduction of Microalbuminuria in Subjects With Type 2 Diabetes Mellitus

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Following a 4-week single-blind placebo run-in period, eligible subjects were randomized in a 1:1 ratio to receive 32 weeks of double-blind study medication: Rosiglitazone (starting dose 4mg od) or Glyburide (starting dose 5mg od), both in combination with open-label Metformin \> or = (1g/day). Subjects were stratified for use of ACEI, nondihydropyridine calcium channel blockers (NDP CCB), or angiotensin II receptor blockers (ARB) to provide equal representation of these subjects in each treatment group.

Study identification

NCT ID
NCT00500955
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
336 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
40 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2000 (Type not available)
Primary completion
Not listed
Completion
Jun 2004 (Actual)
Last update posted
Sep 15, 2016

2000 – 2004

United States locations

U.S. sites
56
U.S. states
26
U.S. cities
51
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35211 —
GSK Investigational Site Tempe Arizona 85282 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Mission Viejo California 92691 —
GSK Investigational Site Pasadena California 91105 —
GSK Investigational Site Redwood City California 94062 —
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site San Diego California 92128 —
GSK Investigational Site Santa Barbara California 93105 —
GSK Investigational Site Tustin California 92780 —
GSK Investigational Site Ukiah California 95482 —
GSK Investigational Site Denver Colorado 80209 —
GSK Investigational Site Denver Colorado 80220 —
GSK Investigational Site New Britain Connecticut 06050 —
GSK Investigational Site Norwalk Connecticut 06850 —
GSK Investigational Site Newark Delaware 19713 —
GSK Investigational Site Jacksonville Florida 32204 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Winter Park Florida 32789 —
GSK Investigational Site Blue Ridge Georgia 30513 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Peoria Illinois 61615 —
GSK Investigational Site Indianapolis Indiana 46201 —
GSK Investigational Site South Bend Indiana 46601 —
GSK Investigational Site Slidell Louisiana 70458 —
GSK Investigational Site Baltimore Maryland 21208 —
GSK Investigational Site Boston Massachusetts 02215 —
GSK Investigational Site Springfield Massachusetts 01199 —
GSK Investigational Site Royal Oak Michigan 48073 —
GSK Investigational Site Brooklyn Center Minnesota 55430 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Henderson Nevada 89014 —
GSK Investigational Site Las Vegas Nevada 89103 —
GSK Investigational Site Albuquerque New Mexico 87106 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site Binghamton New York 13903 —
GSK Investigational Site Endwell New York 13760 —
GSK Investigational Site New York New York 10010 —
GSK Investigational Site Portland Oregon 97232 —
GSK Investigational Site Hermitage Pennsylvania 16148 —
GSK Investigational Site Philadelphia Pennsylvania 19124 —
GSK Investigational Site Pittsburgh Pennsylvania 15221 —
GSK Investigational Site Columbia South Carolina 29201 —
GSK Investigational Site Beaumont Texas 77701 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Houston Texas 77027 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site San Antonio Texas 78207 —
GSK Investigational Site San Antonio Texas 78237 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Edmonds Washington 98026 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Madison Wisconsin 53792 —
GSK Investigational Site Milwaukee Wisconsin 53209-0996 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 57 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00500955, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2016 · Synced Nov 2, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00500955 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →