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A Prospective, Multi-Center, Observational Study to Evaluate the Efficacy of OLMETEC Tab. (or OLMETEC Plus Tab.) on Nocturnal Blood Pressure Control in Korean Patients With Stage Ⅰ Hypertension

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Republic of Korea
Multiple centers in Republic of Korea
RECRUITING
Seoul
Contact Information
Primary
Yun Jeong Kong
yjkong246@daewoong.co.kr
82-10-3206-5162
Time Frame
Start Date: 2025-09-17
Estimated Completion Date: 2027-01-31
Participants
Target number of participants: 12000
Treatments
Olmetec-Based Treatment Cohort
Patients with stage 1 hypertension who are prescribed Olmetec® or Olmetec Plus® as part of routine clinical practice will be included. Patients will be followed prospectively to assess changes in nocturnal blood pressure and blood pressure variability using ambulatory blood pressure monitoring (ABPM). No intervention beyond standard clinical care will be applied.
Related Therapeutic Areas
Sponsors
Leads: Daewoong Pharmaceutical Co. LTD.

This content was sourced from clinicaltrials.gov