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NCT03231293: FABULOUS

Fimasartan Blood Pressure Lowering After Acute Stroke

Completed Last updated 4 November 2019
What this trial tests

trial in Hypertension in 1,035 participants. Completed in 5 April 2019.

Timeline
28 July 2016
Primary endpoint
2 November 2018
5 April 2019

Quick facts

Lead sponsorBoryung Pharmaceutical Co., Ltd
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,035
Start date28 July 2016
Primary completion2 November 2018
Estimated completion5 April 2019
Sites27 locations across South Korea

Conditions studied

Sponsor

Boryung Pharmaceutical Co., Ltd — full company profile →

Who can join

19 and older, any sex, with Hypertension or Ischemic Stroke. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates the effectiveness of fimasartan-based antihypertensive treatment and prognosis in post-acute phase of ischemic stroke or transient ischemic attack patients. All participants will receive fimasartan, and the investigators will follow them up for 6 months.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Fimasartan-Based Blood Pressure Control after Acute Cerebral Ischemia: The Fimasartan-Based Blood Pressure Control after Acute Cerebral Ischemia Study.
    Hong KS, Kwon SU, Park JH, Cha JK, et al · · 2021 · cited 1× · PMID 34184441 · DOI 10.3988/jcn.2021.17.3.344

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Other recruiting trials for Hypertension

Currently open trials in the same condition.

Other Boryung Pharmaceutical Co., Ltd trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03231293.

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