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Completed Phase 3 Interventional Results available

The CLEVER Study - Coreg And Left Ventricular Mass Regression

ClinicalTrials.gov ID: NCT00108082

Public ClinicalTrials.gov record NCT00108082. 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 24, 2026, 5:28 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, Multi-Center Study Comparing the Effects of Carvedilol Modified Release Formulation (COREG MR) and Atenolol in Combination With and Compared to an Angiotensin Converting Enzyme Inhibitor (Lisinopril) on Left Ventricular Mass Regression in Hypertensive Patients With Left Ventricular Hypertrophy (LVH).

Brief summary

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

This study is designed to compare the effects of COREG MR (carvedilol modified release formulation) to atenolol on indices of left ventricular dimensions when added to standardized angiotensin converting enzyme (ACE) inhibition, and to the effect of ACE inhibition alone. Subjects with LVH (left ventricular hypertrophy) and hypertension will be studied. The primary endpoint will be the change in left ventricular mass index (LVMI) characterized by magnetic resonance imaging (MRI) following 12 months of treatment. Secondary endpoints include the change in LV (left ventricular) mass, LV wall thickness, diastolic left ventricular filling parameters, and left ventricular ejection fraction by echocardiographic methods at Treatment Month 12. Composite outcomes and individual event data will also be evaluated by treatment group.

Study identification

NCT ID
NCT00108082
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
287 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
Jan 2005 (Type not available)
Primary completion
Aug 2008 (Actual)
Completion
Aug 2008 (Actual)
Last update posted
Dec 16, 2016

2005 – 2008

United States locations

U.S. sites
78
U.S. states
26
U.S. cities
68
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35235 —
GSK Investigational Site Birmingham Alabama 35249 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Chandler Arizona 77030 —
GSK Investigational Site Mesa Arizona 85206 —
GSK Investigational Site Peoria Arizona 85381 - 4828 —
GSK Investigational Site Scottsdale Arizona 85251 —
GSK Investigational Site Scottsdale Arizona 85260 —
GSK Investigational Site Sun City Arizona 85351 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Los Angeles California 90033 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Palo Alto California 94301 —
GSK Investigational Site Poway California 92064 —
GSK Investigational Site Sacremento California 95819 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site San Leandro California 94578 —
GSK Investigational Site Santa Ana California 92705 —
GSK Investigational Site Colorado Springs Colorado 80907 —
GSK Investigational Site Colorado Springs Colorado 80919 —
GSK Investigational Site Denver Colorado 80204 —
GSK Investigational Site Denver Colorado 80218 —
GSK Investigational Site Newark Delaware 19718 —
GSK Investigational Site Washington D.C. District of Columbia 20037 —
GSK Investigational Site Washington D.C. District of Columbia 20422 —
GSK Investigational Site Altamonte Springs Florida 32714 —
GSK Investigational Site Atlantis Florida 33462 —
GSK Investigational Site Jacksonville Florida 32209 —
GSK Investigational Site Kissimmee Florida 34741 —
GSK Investigational Site Longwood Florida 32779 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Ormond Beach Florida 32714 —
GSK Investigational Site Pembroke Pines Florida 33029 —
GSK Investigational Site Evanston Illinois 60201 —
GSK Investigational Site Vernon Hills Illinois 60061 —
GSK Investigational Site Fort Wayne Indiana 46804 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Scarborough Maine 04074 —
GSK Investigational Site Baltimore Maryland 21224 —
GSK Investigational Site Columbia Maryland 21044 —
GSK Investigational Site Pikesville Maryland 21215 —
GSK Investigational Site Grand Rapids Michigan 49525 —
GSK Investigational Site Edina Minnesota 55435 —
GSK Investigational Site Minneapolis Minnesota 55417 —
GSK Investigational Site Camden New Jersey 08103 —
GSK Investigational Site Buffalo New York 14215 —
GSK Investigational Site New York New York 10011 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10128 —
GSK Investigational Site Williamsville New York 14221 —
GSK Investigational Site Fayetteville North Carolina 28304 —
GSK Investigational Site Greensboro North Carolina 27401 —
GSK Investigational Site Winston-Salem North Carolina 27157 —
GSK Investigational Site Cincinnati Ohio 45224 —
GSK Investigational Site Cincinnati Ohio 45267 —
GSK Investigational Site Cleveland Ohio 44122 —
GSK Investigational Site Hillsboro Oregon 97123-4117 —
GSK Investigational Site Portland Oregon 97210 —
GSK Investigational Site Allentown Pennsylvania 18105 —
GSK Investigational Site Camp Hill Pennsylvania 17011 —
GSK Investigational Site Doylestown Pennsylvania 18901 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Pittsburgh Pennsylvania 15212 —
GSK Investigational Site West Grove Pennsylvania 19390 —
GSK Investigational Site Warwick Rhode Island 02886 —
GSK Investigational Site Columbia South Carolina 29204 —
GSK Investigational Site Greenville South Carolina 29615 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Knoxville Tennessee 37920 —
GSK Investigational Site Nashville Tennessee 37205 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Danville Virginia 24541 —
GSK Investigational Site Roanoke Virginia 24014 —
GSK Investigational Site Springfield Virginia 22151 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Milwaukee Wisconsin 53215 —

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 NCT00108082, 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 Dec 16, 2016 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00108082 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →