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 @ 5:39 PM
Ignite Modification Date: 2025-12-24 @ 5:39 PM
NCT ID: NCT06683768
Eligibility Criteria: Inclusion criteria: 1. Diagnosed with essential hypertension or hypertensive heart/kidney disease at the index date. 2. Sitting systolic blood pressure (sSBP) ≥150 millimeters of mercury (mm Hg) at the index date. 3. At least one prescription of angiotensin-converting enzyme inhibitor (ACEi), angiotensin receptor blocker (ARB), angiotensin receptor neprilysin inhibitor (ARNI), calcium channel blocker (CCB), diuretics, or these SPCs for hypertension at the index date. 4. At least one visit and blood pressure (BP) measurement within 12 weeks from the index date. Exclusion criteria: 1. Prescription of hypertensive medication including alpha blocker, beta blocker, alpha-beta blocker, aldosterone antagonist, and renin inhibitor within 24 weeks prior to the index date. 2. Initial prescription of two or more antihypertensive medicines either with or without SPCs at the index date. 3. History of hypotension, hyperkalemia, hypokalemia, or hyponatremia, drug-related or otherwise, or renal failure leading to dialysis, stroke, myocardial infarction, heart failure at the index date or within 24 weeks prior to the index date. 4. History of secondary hypertension (renal parenchymal hypertension, renovascular hypertension \[unilateral or bilateral renal artery stenosis\] coarctation of the aorta, primary hyperaldosteronism, Cushing's disease, pheochromocytoma, polycystic kidney disease, and drug-induced hypertension, etc.) at any timepoint. 5. Pregnant women at any timepoint.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT06683768
Study Brief:
Protocol Section: NCT06683768