Actively Recruiting
Observational Study to Evaluate the Efficacy of OLMETEC Tab on Nocturnal Blood Pressure Control in Patients With Stage Ⅰ Hypertension
Led by Daewoong Pharmaceutical Co. LTD. · Updated on 2026-04-07
12000
Participants Needed
1
Research Sites
71 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, multicenter, observational study to evaluate the effectiveness of Olmetec® or Olmetec Plus® on nocturnal blood pressure control in Korean patients with stage 1 hypertension. Patients receiving Olmetec-based therapy in routine clinical practice will be followed to assess changes in ambulatory blood pressure, including nocturnal blood pressure and blood pressure variability.
CONDITIONS
Official Title
Observational Study to Evaluate the Efficacy of OLMETEC Tab on Nocturnal Blood Pressure Control in Patients With Stage Ⅰ Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 69 years
- Diagnosed with stage 1 hypertension according to clinical guidelines
- Newly prescribed Olmetec4 or Olmetec Plus4 in routine clinical practice
- Able to undergo ambulatory blood pressure monitoring (ABPM)
- Voluntarily agree to participate and provide written informed consent
You will not qualify if you...
- Patients with secondary hypertension
- Patients with severe hypertension needing immediate pharmacological treatment
- Known allergy to olmesartan medoxomil, hydrochlorothiazide, or any study drug component
- Pregnant, planning pregnancy, or breastfeeding
- Severe kidney or liver impairment
- Unable to comply with study procedures including ambulatory blood pressure monitoring
- Deemed unsuitable for participation by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Multiple centers in Republic of Korea
Seoul, South Korea
Actively Recruiting
Research Team
Y
Yun Jeong Kong
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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