The Impact of Low Sodium Salt Substitute Use on Serum Potassium Levels Among Patients With Hypertension

ConditionHypertension
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohns Hopkins University

About this trial

The goal of this pre-post study is to assess the risk of hyperkalemia in adults with hypertension on medication in Bangladesh. The main questions it aims to answer are:

Is the risk of hyperkalemia after the initiation of Low Sodium Salt Substitute (LSSS) in people on antihypertensive medication (especially RASi) large enough to be concerned about its broad use in this population?

Does initiation of LSSS correct hypokalemia in people on antihypertensive medication (especially RASi) with low serum potassium levels?

Participants will be asked to reduce overall salt intake and to use LSSS on every occasion where regular salt would normally be used, including as cooking salt.

Eligibility criteria

Qualifiers

Adults ≥18 years with clinically diagnosed hypertension treated with medication [on a stable dose at least for 2 months]

Have a phone for contact

Disqualifiers

Those with baseline K ≥5.0 or K <3.0 mmol/L

Advanced kidney disease (eGFR <45 ml/min/1.73m2).

Those on potassium sparing diuretics (e.g., spironolactone)

Other medical conditions determined by physicians (e.g., heart failure treated with medication; life expectancy less than 12 months)

Trial design

Treatments tested in this trial

  • Low-sodium salt substitute

Treatment groups

607 Participants
are divided into 1 treatment group

Sponsors and collaborators

Johns Hopkins University

Lead sponsor

National Heart Foundation of Bangladesh

Collaborator

Vital Strategies

Collaborator