Observational Study to Evaluate the Efficacy of OLMETEC Tab on Nocturnal Blood Pressure Control in Patients With Stage Ⅰ Hypertension
Recruiting
Observational Study
Stage 1 Hypertension
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
19 and older
Sex
Any
Study type
Observational
Participants needed
12,000 (estimated)
Sponsor
Daewoong Pharmaceutical Co. LTD. · Industry
Who this trial is looking for
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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.
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Eligibility Criteria
Inclusion Criteria:
* Adults aged ≥19 years
* Patients diagnosed with stage 1 hypertension according to clinical guidelines
* Patients who are newly prescribed Olmetec® or Olmetec Plus® in routine -clinical practice
* Patients who are able to undergo ambulatory blood pressure monitoring (ABPM)
* Pa…
Inclusion Criteria:
* Adults aged ≥19 years
* Patients diagnosed with stage 1 hypertension according to clinical guidelines
* Patients who are newly prescribed Olmetec® or Olmetec Plus® in routine -clinical practice
* Patients who are able to undergo ambulatory blood pressure monitoring (ABPM)
* Patients who voluntarily agree to participate and provide written informed consent
Exclusion Criteria:
* Patients with secondary hypertension
* Patients with severe hypertension requiring immediate pharmacological i-ntervention
* Patients with known hypersensitivity to olmesartan medoxomil, hydrochlorothiazide, or any component of the study drugs
* Patients who are pregnant, planning to become pregnant, or breastfeeding
* Patients with severe renal impairment or severe hepatic impairment
* Patients who are unable to comply with study procedures, including ABPM
* Patients who are deemed inappropriate for participation by the investigator
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