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Clinical Characteristics and Medication Satisfaction of Kanarb Tablet in Korean Hypertensive Patient(Kanarb-Hypertension Epidemiology Medication Satisfaction Study)

Clinical Characteristics and Medication Satisfaction of Kanarb Tablet in Korean Hypertensive Patient: a Prospective, Cross-sectional and Open-label 8 Week Switching Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02394392
Acronym
K-HEMS
Enrollment
12691
Registered
2015-03-20
Start date
2014-07-31
Completion date
2015-10-31
Last updated
2016-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Medication satisfaction, Quality of life, Drug compliance

Brief summary

1. Investigate the clinical characteristics, medication satisfaction and quality of life of anti-hypertensive drugs in Korean hypertensive patients 2. Observe the changes of medication satisfaction and compliance in patients after switchting to Fimasartan

Interventions

None listed

Sponsors

Boryung Pharmaceutical Co., Ltd
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Step1 * Over 20 years old * Essential hypertensive patients who taking anti-hypertensive drugs during previous 1 month Step2 * Patients does not taking Fimasartan * Patient's medication satisfaction score under 4

Exclusion criteria

* Patients with secondary hypertension * Patients with orthostatic hypotension who has sign and symptom * Patients with known severe or malignancy retinopathy * Patients with significant investigations; abnormal renal function * Childbearing and breast-feeding women * Patients with history of allergic reaction to any angiotensin II antagonist

Design outcomes

Primary

MeasureTime frame
quality of life questionnaire for hypertensionup to 1 month
medication satisfaction questionnaireup to 8 weeks

Secondary

MeasureTime frame
Drug compliance questionnaireup to 8 weeks

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026