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Hypertension screening and treatment program - Article


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Furosemide

Lasix 




Clinical Trial: Hypertension screening and treatment program

This study has been completed.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs

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 Treatment or Intervention
Hypertension
 Drug: Chlorthalidone
 Drug: Furosemide

MedlinePlus related topics:  High Blood Pressure

Study Type: Observational
Study Design: Longitudinal, Defined Population, Prospective Study

Official Title: VA HYPERTENSION SCREENING AND TREATMENT PROGRAM (PILOT STUDY)

Further Study Details: 

Study start: June 1989

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 above,  Genders Eligible for Study:  Both

Criteria

Patients at Hypertension Screening and Treatment Program clinics

Location Information


California
      Vamc - Sepulveda, Sepulveda,  California,  United States

District of Columbia
      Vamc - Washington, Dc, Washington,  District of Columbia,  United States

Florida
      Vamc - Miami, Miami,  Florida,  United States

Indiana
      Vamc - Indianapolis, Indianapolis,  Indiana,  United States

Iowa
      Vamc - Iowa City, Iowa City,  Iowa,  United States

Mississippi
      Vamc - Jackson, Jackson,  Mississippi,  United States

Ohio
      Vamc - Dayton, Dayton,  Ohio,  United States

Pennsylvania
      Vamc - Philadelphia, Philadelphia,  Pennsylvania,  United States

      Vamc - Pittsburgh, Pittsburgh,  Pennsylvania,  United States

Tennessee
      Vamc - Memphis, Memphis,  Tennessee,  United States

Virginia
      Vamc - Richmond, Richmond,  Virginia,  United States

Puerto Rico
      Vamc - San Juan, Pr, San Juan,  Puerto Rico

More Information

Study ID Numbers:  324
Record last reviewed:  February 2003
Last Updated:  October 13, 2004
Record first received:  December 29, 2000
ClinicalTrials.gov Identifier:  NCT00007592
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Resources



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Page Updated: October 3, 2005
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