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An Observation Study on the Identification of Prescription Patterns of Lodient Tab(Telmisartan/S-amlodipine)

An Observation Study on the Identification of Prescription Patterns of Lodient Tab(Telmisartan/S-amlodipine)

Recruiting
19 years and older
All
Phase N/A
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Overview

This study identify prescription patterns of Lodient Tab and evaluate the changes of the hypertension symptoms (BP pressure) who are first prescribed and taking Lodient Tab.

Description

This study aims to observe changes in symptoms according to the treatment effect of hypertension for 6 months after Lodient Tab prescription.

Eligibility

Inclusion Criteria:

  1. Adults over 19 years of age
  2. A person diagnosed with hypertension
  3. A person who has been first prescribed Lodient Tab within the past 4 months as of the IRB approval date or is scheduled to be prescribed Lodient Tab
  4. A person who voluntarily agreed in writing to this study

Exclusion Criteria:

  1. Pregnant women or nursing mothers
  2. Persons subject to prohibition according to the permission of the Lodient Tab
  3. Patients who in the judgement of the investigator, were inappropriate to participate in the study

Study details
    Hypertension

NCT06214832

Hanlim Pharm. Co., Ltd.

29 January 2024

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