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Completed Phase 4 Interventional

Glycemic Control Of Carvedilol Versus Metoprolol In Patients With Type II Diabetes Mellitus And Hypertension

ClinicalTrials.gov ID: NCT00060918

Public ClinicalTrials.gov record NCT00060918. 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 23, 2026, 8:57 PM 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, Multicenter Study Comparing the Glycemic Control Characteristics of Carvedilol and Metoprolol in Hypertensive Patients With Type II Diabetes Mellitus.

Brief summary

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

To evaluate the effects of two different antihypertensive medications in the drug class of beta-blockers on control of glucose in Type II diabetic patients with high blood pressure.

Study identification

NCT ID
NCT00060918
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,210 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
30 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
Jun 2001 (Type not available)
Primary completion
Apr 2004 (Actual)
Completion
Apr 2004 (Actual)
Last update posted
Apr 15, 2015

2001 – 2004

United States locations

U.S. sites
50
U.S. states
20
U.S. cities
46
Facility City State ZIP Site status
GSK Investigational Site Glendale Arizona 85306 —
GSK Investigational Site Phoenix Arizona 85016 —
GSK Investigational Site Phoenix Arizona 85050 —
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site Burlingame California 94010 —
GSK Investigational Site Concord California 94520 —
GSK Investigational Site Encinitas California 92024 —
GSK Investigational Site Hemet California 92543 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Pasadena California 91105 —
GSK Investigational Site Riverside California 92501 —
GSK Investigational Site San Diego California 92102 —
GSK Investigational Site San Luis Obispo California 93405 —
GSK Investigational Site Spring Valley California 91978 —
GSK Investigational Site Aurora Colorado 80045 —
GSK Investigational Site Denver Colorado 80220 —
GSK Investigational Site Golden Colorado 80401 —
GSK Investigational Site Panama City Florida 32401 —
GSK Investigational Site St. Petersburg Florida 33701 —
GSK Investigational Site Honolulu Hawaii 96813 —
GSK Investigational Site Idaho Falls Idaho 83404 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site O'Fallon Illinois 62269 —
GSK Investigational Site Elkhart Indiana 46515 —
GSK Investigational Site Indianapolis Indiana 46260 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Kalamazoo Michigan 49009 —
GSK Investigational Site Oak Park Michigan 48237 —
GSK Investigational Site Minneapolis Minnesota 55417 —
GSK Investigational Site Kansas City Missouri 64106 —
GSK Investigational Site Kansas City Missouri 64111 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site St Louis Missouri 63128 —
GSK Investigational Site Las Vegas Nevada 89103 —
GSK Investigational Site Albuquerque New Mexico 87131 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Bend Oregon 97701 —
GSK Investigational Site Oregon City Oregon 97045 —
GSK Investigational Site Dallas Texas 75390 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Georgetown Texas 78626 —
GSK Investigational Site Midland Texas 79705 —
GSK Investigational Site San Antonio Texas 78259 —
GSK Investigational Site San Antonio Texas 78299 —
GSK Investigational Site The Colony Texas 75056 —
GSK Investigational Site Ogden Utah 84401 —
GSK Investigational Site Renton Washington 98055 —
GSK Investigational Site Madison Wisconsin 53792 —
GSK Investigational Site Milwaukee Wisconsin 53151 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00060918, 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 Apr 15, 2015 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00060918 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →