NCT07907822Not yet recruiting
A Study to Evaluate the Effectiveness and Safety of S-amlodipine-based Monotherapy and Combination Therapy
A Multicenter, Prospective, Observational Study to Evaluate the Effectiveness and Safety of S-amlodipine-based Monotherapy and Combination Therapy in Korean Hypertensive Patients
Source: ClinicalTrials.gov · Last updated 30 Oct 2026
Brief summary (registry, in English)
This study aims to evaluate the effectiveness, safety, and clinical utility as a treatment strategy of the s-amlodipine-based monotherapy, dual combination, and triple combination in patients with hypertension across various stages of blood pressure control in routine clinical practice.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 4528 (estimated)
- First submitted
- 26 Oct 2026
- Start date
- Nov 2026
- Primary completion date
- Feb 2029
- Lead sponsor
- Ahn-Gook Pharmaceuticals Co.,Ltd
- Diseases
- High blood pressure
- NCT number
- NCT07907822
What you commit to
- Study type: Observational
- Planned participants: 4528
- From Nov 2026 to the primary completion date, Feb 2029
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- The patients who are contraindicated for the administration of the study drug according to the approved label
Other
- The patients who meet any of the following exclusion criteria cannot participate in this study.
- The patients who are pregnant, possibly pregnant, or lactating women = The patients who are judged by the investigator to be inappropriate for participation in this study
Who the study is looking for
- Patients who voluntarily consent on the informed consent form and understand the study's purpose, methods, and so on
- Males and females over the age of 19
- Patients who have been diagnosed with essential hypertension and plan to be treated with S- amlodipine or S-amlodipine/Valsartan or S-amlodipine/Valsartan/Indapamide
Age in the registry: 19 years to - · Sex: All
This page is information, not medical advice. Discuss any trial with your doctor.