- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03635255
Circulating microRNAs and Adverse Cardiovascular Outcomes in Patients With Coronary Artery Disease
Study Overview
Status
Conditions
Detailed Description
Objective:To identify the novel circulating miRNA expression profiles that may serve as a sensitive and reliable biomarker to predict future adverse CV outcomes and death in patients with established CAD.
Methods:The investigators propose to utilize next-generation sequencing (RNASeq) to identify the novel plasma miRNA expression signature linked to adverse CV outcomes in participanrs with CAD. The identified miRNA candidates that are predictive of adverse CV events will be validated in a larger independent cohort of CAD patients. In addition, miRNAs that are linked to adverse CV outcomes in CAD patients will be investigated mechanistically in human aortic endothelial cells to understand their functional contribution to the occurrence of adverse CV events.
What is New or Innovative in this Study? This study could be one of the few studies to investigate circulating miRNAs as novel biomarkers for risk stratification and the clinical outcome prediction in patients with established CAD. This report will also demonstrate that some dysregulated circulating miRNAs might contribute to endothelial dysfunction and adverse CV events in CAD patients.
Scientific or Clinical Implication of the Expected Results:The results from this study will provide a new prognostic tool to predict CV outcomes in CAD patients using plasma miRNA expression signature. It will also provide important scientific insights into the complex non-coding RNA regulatory network involved in the pathogenesis of atherosclerosis. The insights from this study may provide a unique opportunity to improve the risk assessment of adverse CV events in CAD patients by targeting theses miRNAs.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Mei chen Huang, Master
- Phone Number: 88559 02-23123456
- Email: ntuh2015@gmail.com
Study Contact Backup
- Name: Chau chung Wu, PhD
- Phone Number: 88560 02-23123456
- Email: Chauchungwu@ntu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan
- Recruiting
- NTUH
-
Contact:
- Chau chuna Wu
- Phone Number: 88560 886-2-23123456
- Email: chauchungwu@ntu.edu.tw
-
Contact:
- MeiChen Huang
- Phone Number: 88559 886-2-23123456
- Email: ntuh2015@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
- Male or female older than 20 years old.
- Have a history of cardiovascular disease (including coronary heart disease, or peripheral vascular disease)
Description
Inclusion Criteria:
- Male or female older than 20 years old.
- Have a history of cardiovascular disease (including coronary heart disease, or peripheral vascular disease)
Exclusion Criteria:
Significant valvular or congenital heart disease, cancer, immunosuppressive therapy, or other conditions or treatment your physician thinks you have
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
composite cardiovascular outcome
Time Frame: up to 10 years
|
Circulating microRNAs and Adverse Cardiovascular Outcomes in Patients
|
up to 10 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Chau chung Wu, PhD, National Taiwan University Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201708063RIND
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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