Skip to content

Effects of Potassium Salts on Blood Pressure and Target Organ Damage

Effect of Potassium Bicarbonate and Potassium Chloride on Blood Pressure and Markers of Target Organ Damage in Hypertensives

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00160368
Enrollment
45
Registered
2005-09-12
Start date
2005-01-31
Completion date
2008-03-31
Last updated
2007-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Hypertension, potassium salts

Brief summary

The purpose of this study is to determine the effect of potassium chloride and potassium bicarbonate on blood pressure and also to determine whether increasing potassium intake has beneficial effects on the surrogate markers of target organ damage in cardiovascular disease, as well as on bone health.

Detailed description

Randomised trials have shown that increasing potassium intake lowers blood pressure. However, most previous trials used potassium chloride. Whereas, potassium in fruits and vegetables is not a chloride salt, but a mixture of potassium phosphate, sulphate, citrate, and many organic anions, most of which are precursors of potassium bicarbonate. It is unclear whether non-chloride salt of potassium has greater or lesser effect on blood pressure compared to potassium chloride. Experimental studies in animals and epidemiological studies in humans suggest that a high potassium intake may have beneficial effects on the cardiovascular system and the kidney, independent of its effect on blood pressure, and also reduce the risk of osteoporosis. We propose to carry out a randomised double-blind trial to compare potassium bicarbonate with potassium chloride looking at their effect on blood pressure, and also to determine whether these potassium salts have beneficial effects on the cardiovascular system, kidney and bone health. Comparisons: potassium chloride vs potassium bicarbonate vs placebo.

Interventions

Sponsors

St George's, University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with untreated essential hypertension (sitting systolic blood pressure between 140 and 170 mmHg and/or sitting diastolic blood pressure between 90 and 105 mmHg); * Age 18 - 75 years.

Exclusion criteria

* Individuals younger than 18 or older than 75 years; * Individuals with impaired renal function with plasma creatinine greater than 120 umol/L for non-blacks or 150 umol/L for blacks; * Individuals with chronic diarrhea, or history of peptic ulcer; * Individuals with baseline plasma potassium values greater than 5.0 mmol/L; * Individuals with severe hypertension i.e. blood pressure \> 170/105 mmHg; * Individuals with diabetes mellitus; * Individuals with any secondary cause of hypertension; * Individuals with malignancy or liver disease; * Individuals with ischaemic heart disease or heart failure; * Females who are pregnant or breast feeding or on the oral contraceptive pill.

Design outcomes

Primary

MeasureTime frame
Blood pressure and markers of target organ damage and bone health at 4 weeks of potassium supplementation.

Secondary

MeasureTime frame
Comparisons among different treatments in blood pressure and markers of target organ damage and bone health.

Countries

United Kingdom

Contacts

Primary ContactFeng J He, PhD
fhe@sgul.ac.uk0044-20-8725-5375
Backup ContactGraham A MacGregor, MD
gmacgregor@sgul.ac.uk0044-20-8725-5774

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026