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Terminated Phase 3 Interventional

COREG MR Versus TOPROL-XL On Reduction Of Microalbuminuria In Patients With Hypertension And Microalbuminuria

ClinicalTrials.gov ID: NCT00123903

Public ClinicalTrials.gov record NCT00123903. 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 Oct 25, 2026, 12:32 AM EDT

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

Official title

A Randomized, Double-blind, Positive-Controlled, Multicenter Study Comparing the Efficacy of Carvedilol Phosphate Modified Release Formulation (COREG MR) and Metoprolol Succinate Extended Release (TOPROL-XL) on the Reduction of Microalbuminuria in Patients With Hypertension and Microalbuminuria

Brief summary

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

This study was designed to determine whether COREG MR is more effective than TOPROL-XL in reducing microalbuminuria in type 2 diabetic or non-diabetic patients with high blood pressure and microalbuminuria.

Study identification

NCT ID
NCT00123903
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,220 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Jul 2005 (Type not available)
Primary completion
May 2006 (Actual)
Completion
May 2006 (Actual)
Last update posted
Jan 18, 2017

2005 – 2006

United States locations

U.S. sites
72
U.S. states
24
U.S. cities
63
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35213 —
GSK Investigational Site Mobile Alabama 36617 —
GSK Investigational Site Phoenix Arizona 85023 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Inglewood California 90301 —
GSK Investigational Site Los Angeles California 90057 —
GSK Investigational Site Mission Viejo California 92691 —
GSK Investigational Site Oakland California 94609 —
GSK Investigational Site Redondo Beach California 90277 —
GSK Investigational Site Colorado Springs Colorado 80919 —
GSK Investigational Site Hollywood Florida 33023 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Miami Florida 33169 —
GSK Investigational Site Pembroke Pines Florida 33024 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Decatur Georgia 30035 —
GSK Investigational Site Chicago Illinois 60607 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Melrose Park Illinois 60160 —
GSK Investigational Site Avon Indiana 46123 —
GSK Investigational Site Elkhart Indiana 46515 —
GSK Investigational Site Evansville Indiana 47713 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site Indianapolis Indiana 46250 —
GSK Investigational Site Indianapolis Indiana 46254 —
GSK Investigational Site Lafayette Louisiana 70503 —
GSK Investigational Site Ayer Massachusetts 01432 —
GSK Investigational Site Worcester Massachusetts 01608 —
GSK Investigational Site Las Vegas Nevada 89119 —
GSK Investigational Site Voorhees Township New Jersey 08043 —
GSK Investigational Site Buffalo New York 14222 —
GSK Investigational Site Camillus New York 13031 —
GSK Investigational Site East Syracuse New York 13057 —
GSK Investigational Site Kingston New York 12401 —
GSK Investigational Site Port Chester New York 10573 —
GSK Investigational Site Rochester New York 14618 —
GSK Investigational Site Charlotte North Carolina 28211 —
GSK Investigational Site Greensboro North Carolina 27401 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Cleveland Ohio 44130 —
GSK Investigational Site Columbus Ohio 43210-1296 —
GSK Investigational Site Kettering Ohio 45429 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Oregon City Oregon 97045 —
GSK Investigational Site Beaver Pennsylvania 15009 —
GSK Investigational Site Havertown Pennsylvania 19083 —
GSK Investigational Site Philadelphia Pennsylvania 19152 —
GSK Investigational Site Reading Pennsylvania 19601 —
GSK Investigational Site West Grove Pennsylvania 19390 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Johnson City Tennessee 37604 —
GSK Investigational Site Beaumont Texas 77701 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75390-9068 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Galveston Texas 77555-0188 —
GSK Investigational Site Houston Texas 77024 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Midland Texas 79705 —
GSK Investigational Site San Antonio Texas 78216 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Burke Virginia 22015 —
GSK Investigational Site Springfield Virginia 22151 —
GSK Investigational Site Edmonds Washington 98026 —
GSK Investigational Site Olympia Washington 98502 —
GSK Investigational Site Spokane Washington 99206 —
GSK Investigational Site Spokane Washington 99207 —
GSK Investigational Site Spokane Washington 99208 —
GSK Investigational Site Wenatchee Washington 98801 —

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00123903, 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 Jan 18, 2017 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00123903 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →