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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04174456
Other study ID # 18-215
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date December 31, 2021

Study information

Verified date August 2020
Source Dong-A University
Contact Kyung-Mi Ko
Phone 82-51-240-5740
Email kkmcrc@naver.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 31, 2021
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- dilated cardiomyopathy

Exclusion Criteria:

- contraindication to angiotensin receptor blocker

- cardiogenic shock

- sensitive to rosuvastatin

- liver cirrhosis more than Child class B

Study Design


Intervention

Diagnostic Test:
FDG PET
baseline and 6-month follow-up FDG PET

Locations

Country Name City State
Korea, Republic of Department of Internal Medicine,Dong-A University College of Medicine Busan

Sponsors (1)

Lead Sponsor Collaborator
Dong-A University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of glucose metabolism data from fludeoxyglucose positron emission tomography 6 month
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