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Study of the Fimasartan effects on cardiovascular events and metabolic syndrome in patients with hypertension

Study of the Fimasartan effects on cardiovascular events and metabolic syndrome in patients with hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0000529
Enrollment
20000
Registered
2012-09-07
Start date
2011-10-18
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Cheil General Hospital & Women's healthcare center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with hypertension who are 20 years old and higher and need angiotensin ? receptor blockers(ARBs), Fimasartan(Kanarb) 2.Patients who agreed to this study and handed out written consent forms 3.Patients who visited after fasting

Exclusion criteria

Exclusion criteria: 1. Patients who are currently taking Kanarb

Design outcomes

Primary

MeasureTime frame
the frequency and incidence of major adverse cardiovascular event(MACE) in the treated kanarb during average 3 years of follow-up visits using a cohort study with office hypertension

Secondary

MeasureTime frame
Changes in degree of metabolic risk after 3 months of follow-up observation.;A incidence of metabolic syndrome and diabetes after 1-year follow-up ;Effect of blood pressure changes and side effects according to presence or absence of metabolic syndrome;Difference of clinic and home blood pressure after Kanarb treatment;changes of incidence of white coat and masked hypertension after Kanarb treatment;Changes of blood pressure variability after Kanarb treatment

Countries

Korea, Republic of

Contacts

Public ContactSuk Jeong

Cheil General Hospital & Women's healthcare center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026