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Taking people in South KoreaNo phase

Effectiveness and Safety of Sequential Triple Combination Therapy (Amlodipine/Losartan/Chlorthalidone) in Korean Patients With Hypertension

Key facts

Where
Gyeonggi-do, South KoreaSee the site

Where in South Korea

  • Yongin Severance HospitalGyeonggi-do, South KoreaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Hanmi Pharmaceutical Company Limited
Trial code
NCT07784296
Record updated
25 August 2026
Original description
A multicenter, prospective, non-interventional, observational study to evaluate effectiveness and safety of sequential triple combination therapy (amlodipine/losartan/chlorthalidone) in Korean patients with hypertensionRead full original descriptionShow less

A Multicenter, Prospective, Non-interventional, Observational Study to Evaluate Effectiveness and Safety of Sequential Triple Combination Therapy (Amlodipine/Losartan/Chlorthalidone) in Korean Patients With Hypertension

A multicenter, prospective, non-interventional, observational study to evaluate effectiveness and safety of sequential triple combination therapy (amlodipine/losartan/chlorthalidone) in Korean patients with hypertension

Inclusion: Korean patients aged 19 years or older diagnosed with hypertension; Individuals newly diagnosed with hypertension or currently taking a single antihypertensive drug; Individuals for whom administration of Amoprel tablets has been determined based on the researcher's medical judgment; Individuals who have heard an explanation of this study and have voluntarily given written consent to participate in the study.

Exclusion: Individuals falling under the contraindications listed in the precautions for use of Amoprel Tab. or Amozartan Plus Tab; Pregnant women, women who may be pregnant, and nursing mothers; Individuals currently participating in an interventional study; Individuals deemed unsuitable for participation in this study by the researcher for other reasons.

ClinicalTrials.gov NCT07784296