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Hypertension Screening and Treatment Program

This study has been completed.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00007592
  Purpose

Hypertension is one of the most common medical problems in the United States and in the VA health care system. It has been well-documented that hypertension can be effectively treated. However, there remain important unresolved clinical questions in the area of antihypertensive treatment. For example, how much is mortality affected by visit compliance, blood pressure control and type of antihypertensive agent? Or, are some regimens associated with more morbidity than others? Or, are there inexpensive regimens that are as effective as more expensive regimens? The amount of data that is available from this demonstration project (currently 6,100 patients) will help address these questions. The answers to these questions should result in better care for veterans with hypertension.


Condition Intervention
Hypertension
Drug: Chlorthalidone
Drug: Furosemide

MedlinePlus related topics:   High Blood Pressure   

ChemIDplus related topics:   Furosemide    Chlorthalidone   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Longitudinal, Defined Population, Prospective Study
Official Title:   VA HYPERTENSION SCREENING AND TREATMENT PROGRAM (PILOT STUDY)

Further study details as provided by Department of Veterans Affairs:

Study Start Date:   June 1989

Detailed Description:

Primary Hypothesis: A variety of clinical questions of major importance can be addressed using clinical data routinely obtained in the VA Hypertension Screening and Treatment Program. For example, treatment of mild hypertension reduces the risk of strokes and heart attacks.

Secondary Hypothesis: Target organ damage occurs despite blood pressure control.

Intervention: Chlorthalidone, furosemide, hydrochlorothiazide, metolazone, indapamide, amiloride, spironolactone, triamterene, atenolol, metoprolol, nadolol, pindolol, propranolol, timolol, acebutolol, penbutolol, clonidine, guanethidine, methydopa, prazosin, guanadrel, labetalol, reserpine, guanfacine, hydralazine, minoxidil, captopril, enalapril, lisinopril, diltiazem, nifedipine, verapamil, nicardipine, dyazide, maxzide, pargyline, terazosin, other anti-hypertensives.

Primary Outcomes: Blood Pressure and Target Organ Damage

Study Abstract: Hypertension is one of the most common medical problems in the United States and in the VA health care system. It has been well-documented that hypertension can be effectively treated. However, there remain important unresolved clinical questions in the area of antihypertensive treatment. For example, how much is mortality affected by visit compliance, blood pressure control and type of antihypertensive agent? Or, are some regimens associated with more morbidity than others? Or, are there inexpensive regimens that are as effective as more expensive regimens? The amount of data that is available from this demonstration project (currently 6,100 patients) will help address these questions. The answers to these questions should result in better care for veterans with hypertension.

This demonstration project provides for central collection of a standard set of clinical data for patients at some of the Hypertension Screening and Treatment Program clinics, thereby setting up a national data base on the treatment of hypertension. The primary objective of this project is to demonstrate the value of establishing this type of database. The database is being used to estimate the average annual cost of different antihypertensive regimens, to determine the cost-efficacy of different therapies and the least expensive effective therapy and to address some major unanswered clinical questions that require large populations and long-term patient care data. There are currently 13 medical centers participating.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Patients at Hypertension Screening and Treatment Program clinics

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00007592

Locations
United States, California
Vamc - Sepulveda    
      Sepulveda, California, United States
United States, District of Columbia
Vamc - Washington, Dc    
      Washington, District of Columbia, United States
United States, Florida
Vamc - Miami    
      Miami, Florida, United States
United States, Indiana
Vamc - Indianapolis    
      Indianapolis, Indiana, United States
United States, Iowa
Vamc - Iowa City    
      Iowa City, Iowa, United States
United States, Mississippi
Vamc - Jackson    
      Jackson, Mississippi, United States
United States, Ohio
Vamc - Dayton    
      Dayton, Ohio, United States
United States, Pennsylvania
Vamc - Philadelphia    
      Philadelphia, Pennsylvania, United States
Vamc - Pittsburgh    
      Pittsburgh, Pennsylvania, United States
United States, Tennessee
Vamc - Memphis    
      Memphis, Tennessee, United States
United States, Virginia
Vamc - Richmond    
      Richmond, Virginia, United States
Puerto Rico
Vamc - San Juan, Pr    
      San Juan, Puerto Rico

Sponsors and Collaborators
  More Information


Study ID Numbers:   324
First Received:   December 29, 2000
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00007592
Health Authority:   United States: Federal Government

Keywords provided by Department of Veterans Affairs:
Hypertension  
national data base on the treatment of hypertension  
cost of different antihypertensive regimens  

Study placed in the following topic categories:
Chlorthalidone
Vascular Diseases
Furosemide
Hypertension

Additional relevant MeSH terms:
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Natriuretic Agents
Therapeutic Uses
Physiological Effects of Drugs
Diuretics
Sodium Chloride Symporter Inhibitors
Cardiovascular Diseases
Cardiovascular Agents
Sodium Potassium Chloride Symporter Inhibitors
Antihypertensive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 03, 2008




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