Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT07465549

CART BP Pro-Guided Blood Pressure Management for Uncontrolled Hypertension

Led by Korea University Anam Hospital · Updated on 2026-04-30

400

Participants Needed

3

Research Sites

92 weeks

Total Duration

On this page

Sponsors

K

Korea University Anam Hospital

Lead Sponsor

D

Daewoong Pharmaceutical Co. LTD.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This multicenter, prospective, open-label randomized controlled trial evaluates the efficacy and safety of CART BP Pro-guided blood pressure management in Korean patients with uncontrolled hypertension. CART BP Pro is a wearable cuffless blood pressure monitoring device based on photoplethysmography technology that enables continuous ambulatory blood pressure monitoring. Eligible participants with uncontrolled hypertension despite ongoing antihypertensive therapy will be randomly assigned in a 1:1 ratio to either a CART BP Pro-guided management group or a usual care group based on conventional office blood pressure measurements. Antihypertensive treatment in both groups will follow guideline-based therapy using standard agents including angiotensin receptor blockers, calcium channel blockers, and thiazide diuretics. The primary efficacy endpoint is the between-group difference in 24-hour mean systolic blood pressure at 24 weeks measured using ambulatory blood pressure monitoring. Safety will be assessed by the incidence of treatment-emergent adverse events during the study period.

CONDITIONS

Official Title

CART BP Pro-Guided Blood Pressure Management for Uncontrolled Hypertension

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 19 years or older
  • Uncontrolled hypertension defined as office systolic blood pressure 140 mmHg or higher or diastolic blood pressure 90 mmHg or higher
  • Ability and willingness to provide written informed consent and comply with study procedures
Not Eligible

You will not qualify if you...

  • History of intolerance or contraindication to olmesartan, amlodipine, or hydrochlorothiazide
  • Suspected secondary hypertension
  • Atrial fibrillation
  • Pregnancy or lactation
  • Any serious medical condition that may interfere with study participation or interpretation of study results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Korea University Ansan Hospital

Ansan, South Korea

Actively Recruiting

2

Korea University Anam Hospital

Seoul, South Korea, 02841

Actively Recruiting

3

Korea University Guro Hospital

Seoul, South Korea

Actively Recruiting

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Research Team

H

Hyung Joon Joo, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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