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Combination of Olmesartan Effect on Myocardial Viability of Patients With Dilated Cardiomyopathy

Olmesartan Effect on Myocardial Viability of Patients With Dilated Cardiomyopathy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04174456
Enrollment
40
Registered
2019-11-22
Start date
2019-12-01
Completion date
2021-12-31
Last updated
2020-08-26

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

Conditions

Dilated Cardiomyopathy

Brief summary

The study proceeds with prospective, randomized, open and controlled clinical trials. The subject of the investigator's study was the first patient diagnosed with dilated cardiomyopathy. Subjects who agreed to participate in the study and were determined to meet the selection / exclusion criteria were randomly assigned to each group, and the experimental group was treated with 20 mg of olmesartan and 5 mg of rosuvastatin for 6 months, and the control group is treated with 40 mg of valsartan and 5 mg of rosuvastatin.

Detailed description

Myocardial viability plays an important role in improving the function of the heart. To date, the most reproducible and objective method has been established as a method or tool for assessing myocardial viability. Olmesartan is known to have the strongest inhibitory ability of angiotensin receptors compared with other angiotensin receptor binding inhibitors. Research has been reported that statin drugs may help improve vascular endothelial function, and several researchers have suggested that these mechanisms may affect the improvement of myocardial survival. In addition, studies have shown that angiotensin receptor binding inhibitors and statins may improve left ventricular function in patients with left ventricular function. However, since the studies did not assess myocardial survival, the mechanisms could not be clearly identified. The purpose of this study is to investigate the effect of olmesartan on myocardial survival in patients with dilated cardiomyopathy who have left ventricular dysfunction.

Interventions

DIAGNOSTIC_TESTFDG PET

baseline and 6-month follow-up FDG PET

Sponsors

Dong-A University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* dilated cardiomyopathy

Exclusion criteria

* contraindication to angiotensin receptor blocker * cardiogenic shock * sensitive to rosuvastatin * liver cirrhosis more than Child class B

Design outcomes

Primary

MeasureTime frameDescription
Rate of glucose metabolism6 monthdata from fludeoxyglucose positron emission tomography

Countries

South Korea

Contacts

Primary ContactKyung-Mi Ko
kkmcrc@naver.com82-51-240-5740

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026