Potassium Chloride Effervescent |
Effer-K; Effervescent Potassium; Gen-K Powder; K+ Care; K-Lor Powder; K-Lyte; K-Lyte/Cl; Kay Ciel Powder; Klor-Con/EF; Klorvess |
Clinical Trial: Potassium and Sodium to Control Blood Pressure in Hypertensives
This study has been completed.
Purpose
To examine the role of dietary sodium reduction with and without potassium supplementation in controlling blood pressure in hypertensive men.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Cardiovascular Diseases Heart Diseases Hypertension Vascular Diseases | Behavior: diet, sodium-restricted Behavior: diet, potassium-supplementation | Phase III |
MedlinePlus related topics: Heart Diseases; Heart Diseases--Prevention; High Blood Pressure; Vascular Diseases
Study Type: Interventional
Study Design: Treatment, Randomized, Parallel Assignment
Study start: September 1983
BACKGROUND: Appropriately increased interest and concern about high blood pressure as a major public health problem coincided with the indication that the risks of hypertension-related morbidity and mortality could be reduced by reduction of blood pressure. Consensus suggestions that individualized approaches be used in treating patients with mild hypertension stimulated further investigations of non-pharmacological methods. Such investigations were also of considerable interest in relation to understanding the physiology of blood pressure control as well as the development of less costly non-drug therapies. Interest was heightened by information suggesting that there might be distinctly harmful side effects related to antihypertensive drug therapy, particularly thiazide diuretics, in some settings. Studies of non-drug therapies included dietary modifications primarily involving weight reduction and sodium restriction with increasing recent concern about other factors such as alcohol intake, dietary fat, calcium, magnesium, and potassium intake.
DESIGN NARRATIVE: Randomized, double-blind. One hundred forty-five subjects were randomized into a low sodium placebo group in which sodium intake was restricted to no more than 80 mEq/day, 142 subjects into a potassium supplementation (96 mEq/day) group whose sodium intake was also restricted to no more than 80 mEq/day. After 12 weeks of intervention, antihypertensive drugs were withdrawn. Follow-up of each participant was for at least two years. The primary endpoint was the proportion of subjects requiring antihypertensive medication at various points following randomization.
Eligibility
Ages Eligible for Study: 45 Years - 68 Years, Genders Eligible for Study: Male
Criteria
More Information
Publications
Grimm RH, Kofron PM, Neaton JD, Svendsen KH, Elmer PJ, Holland L, Witte L, Clearman D, Prineas RJ. Effect of potassium supplementation combined with dietary sodium reduction on blood pressure in men taking antihypertensive medication. J Hypertens Suppl. 1988 Dec;6(4):S591-3.
Grimm RH Jr, Neaton JD, Elmer PJ, Svendsen KH, Levin J, Segal M, Holland L, Witte LJ, Clearman DR, Kofron P, et al. The influence of oral potassium chloride on blood pressure in hypertensive men on a low-sodium diet. N Engl J Med. 1990 Mar 1;322(9):569-74.
Record last reviewed: January 2000
Last Updated: October 13, 2004
Record first received: October 27, 1999
ClinicalTrials.gov Identifier: NCT00000509
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Effer-K (Drug Digest)
- Effervescent Potassium (Drug Digest)

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