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Efficacy of Coreg CR and Lisinopril on Markers for Cardiovascular Functional and Structural Disease (DETECT)

Primary Purpose

Pre-hypertension

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
carvedilol phosphate
lisinopril
carvedilol phosphate and lisinopril
placebo and placebo
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pre-hypertension focused on measuring cardiovascular disease prevention

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males and females > 18 years old with pre-hypertensive or borderline blood pressures (systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85 mmHg) deemed not to need antihypertensive therapy. Subjects must also have one additional risk factor for cardiovascular disease, including:
  • LDL > 130 and < 160 mg/dL
  • HDL < 40 mg/dL
  • Fasting blood sugar >100 and < 126 mg/dL
  • Body mass index ≥ 30
  • Smoker
  • Family history of premature heart disease or hypertension

Exclusion Criteria:

  • Patients with a history of cardiac, cerebral or other vascular events within the previous 6 months will be excluded. Other exclusions include background therapy with a beta blocker or ACE inhibitor therapy, known or suspected intolerance to beta blockers or ACE inhibitors, angiotensin receptor blocker therapy, or diabetes. Pregnant or lactating women, and women of child-bearing age who are not using an acceptable form of contraception are also excluded from this study.

Sites / Locations

  • University of Minnesota, Variety Club Research Center 102

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

1

2

3

4

Arm Description

Coreg CR + lisinopril

Coreg CR + placebo

lisinopril + placebo

placebo + placebo

Outcomes

Primary Outcome Measures

Change in Disease Score (DS) Among the Treatment Groups
Rasmussen Disease Score (RDS) Change From Baseline to 9 Months A score of six or higher on these tests means the patient likely has plaque build-up in the arteries, or atherosclerosis, while a score of three to five suggests that such a problem may be developing. A score of two or less signals a patient is fine but should return in the future for another test. The method detects disease at the earliest moment, before the traditionally used calcium score would show any signs of trouble.

Secondary Outcome Measures

Full Information

First Posted
November 5, 2007
Last Updated
March 23, 2018
Sponsor
University of Minnesota
Collaborators
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00553969
Brief Title
Efficacy of Coreg CR and Lisinopril on Markers for Cardiovascular Functional and Structural Disease
Acronym
DETECT
Official Title
Efficacy of Coreg CR and Lisinopril on Markers for Cardiovascular Functional and Structural Disease. DETECT (DEtection and Treatment of Early Cardiovascular Disease Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
GlaxoSmithKline

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the individual and combined effects of Coreg CR and lisinopril, on cardiovascular health as measured by Rasmussen Disease Score (RDS) in a blinded, placebo controlled comparison over a 9-month study period. Patients to be randomized will have pre-hypertensive blood pressures that do not require anti-hypertensive therapy and at least one additional cardiovascular risk factor.
Detailed Description
This study will compare the effect of Coreg CR and lisinopril, separately and together, on Rasmussen Disease Score in a controlled study with an inactive substance (placebo). Study patients will have pre-hypertensive (slightly elevated) blood pressures not requiring therapy. Lisinopril is an angiotensin converting enzyme (ACE) inhibitor. Angiotensin is a chemical that is made by the body continuously. Angiotensin narrows blood vessels and thereby maintains (elevates) blood pressure. When the enzyme is blocked by lisinopril, angiotensin cannot be converted into its active form. As a result, blood pressure is lowered. Lisinopril is a drug that has been approved for use by the U.S. Food and Drug Administration (FDA) and health authorities for the treatment of high blood pressure and heart failure. Coreg CR is a once-a-day heart medication that is part of a class of drugs known as beta-blockers. Beta-blockers prevent beta-adrenergic substances such as adrenaline from activating parts of the nervous system, including the heart. Beta-blockers therefore relieve stress on the heart by slowing heart beat, decreasing the force of heart muscle contractions, and reducing blood pressure. Coreg has also been approved by the FDA for the treatment of hypertension and various other cardiovascular conditions. It is possible that the beta blocker could increase the benefits of the ACE inhibitor by inhibiting renin production, which is an important step in angiotensin production. These two drugs may act together to provide even more protection to blood vessels and the heart.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-hypertension
Keywords
cardiovascular disease prevention

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
101 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Coreg CR + lisinopril
Arm Title
2
Arm Type
Experimental
Arm Description
Coreg CR + placebo
Arm Title
3
Arm Type
Experimental
Arm Description
lisinopril + placebo
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
placebo + placebo
Intervention Type
Drug
Intervention Name(s)
carvedilol phosphate
Other Intervention Name(s)
Coreg CR
Intervention Description
Extended release capsules, 20mg once daily for 1 month, 40mg once daily for 8 months
Intervention Type
Drug
Intervention Name(s)
lisinopril
Intervention Description
tablets, 10mg once daily for 1 month, 20mg once daily for 8 months
Intervention Type
Drug
Intervention Name(s)
carvedilol phosphate and lisinopril
Other Intervention Name(s)
Coreg CR (carvedilol phosphate)
Intervention Description
carvedilol phosphate = extended release capsules, 20mg once daily for 1 month, 40mg once daily for 8 months; lisinopril= tablets, 10mg once daily for 1 month, 20mg once daily for 8 months
Intervention Type
Drug
Intervention Name(s)
placebo and placebo
Intervention Description
capsule once daily for 9 months; dosage unknown
Primary Outcome Measure Information:
Title
Change in Disease Score (DS) Among the Treatment Groups
Description
Rasmussen Disease Score (RDS) Change From Baseline to 9 Months A score of six or higher on these tests means the patient likely has plaque build-up in the arteries, or atherosclerosis, while a score of three to five suggests that such a problem may be developing. A score of two or less signals a patient is fine but should return in the future for another test. The method detects disease at the earliest moment, before the traditionally used calcium score would show any signs of trouble.
Time Frame
Baseline and nine months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females > 18 years old with pre-hypertensive or borderline blood pressures (systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85 mmHg) deemed not to need antihypertensive therapy. Subjects must also have one additional risk factor for cardiovascular disease, including: LDL > 130 and < 160 mg/dL HDL < 40 mg/dL Fasting blood sugar >100 and < 126 mg/dL Body mass index ≥ 30 Smoker Family history of premature heart disease or hypertension Exclusion Criteria: Patients with a history of cardiac, cerebral or other vascular events within the previous 6 months will be excluded. Other exclusions include background therapy with a beta blocker or ACE inhibitor therapy, known or suspected intolerance to beta blockers or ACE inhibitors, angiotensin receptor blocker therapy, or diabetes. Pregnant or lactating women, and women of child-bearing age who are not using an acceptable form of contraception are also excluded from this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay N Cohn, MD
Organizational Affiliation
Professor, University of Minnesota, Cardiology Division
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota, Variety Club Research Center 102
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

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Efficacy of Coreg CR and Lisinopril on Markers for Cardiovascular Functional and Structural Disease

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