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NCT02958631 Clinical Trial

Comparison of Blood Pressure Lowering Effect Between Fimasartan and Losartan

Hypertension Clinical Trial

Official title:
Comparison of Blood Pressure Lowering Effect Between Fimasartan and Losartan in the Hypertensive Patient During Night and Early Morning Time

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT02958631
Other study ID # CEFILONE Study
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received November 5, 2016
Last updated November 5, 2016
Start date November 2014
Est. completion date April 2017

Study information
Verified date November 2016
Source Chuncheon Sacred Heart Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Comparison of blood pressure lowering effect between Fimasartan and Losartan in the hypertensive patient during night and early morning time

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 40
Est. completion date April 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Subject don't have Anti-hypertensive drug or who stop Anti-hypertensive drug during 2 weeks

- Office BP: over siSBP 140mmHg or si DBP 90mmHg

- 24hr ABPM: SBP 130mmHg or DBP 80mmHg (24 hour Average)

Exclusion Criteria:

- Pregnant, trying to become pregnant or breast feeding

- Subject has Secondary Hypertension

- White coat Blood Pressure (Normal result of 24 hour ABPM)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Fimasartan

• Losartan

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Chuncheon Sacred Heart Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary Blood Pressure Lowering Effect through 24 ABPM comparing blood pressure lowering effect between night and early morning 24 hour No
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