Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 3:06 PM
Ignite Modification Date: 2025-12-24 @ 3:06 PM
NCT ID: NCT03909659
Eligibility Criteria: Inclusion Criteria: * Male or female aged 18 years or over * History of hypertension diagnosed by a health professional - hypertension may be self-reported and antihypertensive drugs may or may not be used for management. There is no entry criterion based upon blood pressure measurements made at the baseline survey * Eat most of their meals in the home * Consent to participate Exclusion Criteria: * Participant or family member is using a potassium-sparing diuretic * Participant or family member is using a potassium supplement * Participant or family member has known significant renal dysfunction * Participant or family member has other reason for concern about use of salt substitute * Participant is not expected to live longer than 6 months from the date of assessment * Another member of the household is already enrolled in the study
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT03909659
Study Brief:
Protocol Section: NCT03909659