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Clinical Trials/NCT03170830
NCT03170830UnknownNot Applicable

Study on CircRNA-Uck2 as a New Diagnostic Marker of Acute Myocardial Infarction

Beijing Haidian Hospital1 site in 1 country178 target enrollmentStarted: August 1, 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
178
Locations
1
Primary Endpoint
The change of cUck2 levels in AMI

Study Overview

Brief Summary

This is an observational diagnostic study that aims to evaluate the diagnostic value of circRNA-Uck2 in Acute Myocardial Infarction (AMI) in adults as compared to healthy and unstable angina controls. Rapid and adequate diagnosis of AMI is of great importance to enable a rapid start of treatment, save large tracts of dying myocardium, reduce the infarct size,and thereby decrease the risk of subsequent heart failure.

Detailed Description

RATIONAL acute myocardial infarction (AMI) is the leading cause of sudden death and heart failure worldwide. And about 10% of all emergency department consultations are with symptoms suggestive of AMI, however, only 10% to 20% of them are diagnosed as experiencing an AMI. Rapid and accurate identification of AMI is of paramount clinical importance for subsequent timely and effectively treatment and management.

Recently, the investigators identified microarray analysis and real-time polymerase chain reaction (PCR) from AMI animal models and small samples of AMI patients, a molecular signature of AMI involving 5 circRNAs (circRNA_006877, circRNA_015350, circRNA_002969, circRNA_013240, circRNA_004682) was found significantly change in AMI patients and likely serves as candidate serum biomarkers of AMI. Among the 5 circRNAs, circRNA_006877 name of circRNA-Uck2 (cUck2) has more close association with AMI.

TYPE OF STUDY : multicenter diagnostic evaluation Study MAIN PURPOSE OF THE STUDY : To evaluate the diagnostic value of circRNAs in AMI in adults as compared to healthy and unstable angina controls

SECONDARY OBJECTIVES :

assess the ability of cUck2 to discriminate a AMI disease from unstable angina patients in adults.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Participant)

Masking Description

Sample inspector

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Health Control Group:Pepole who have normal ECG, deny the history of cardiovascular disease can be included in the healthy control group.
  • Acute Myocardial Infarction Group:Clinical diagnosis of acute myocardial infarction
  • Unstable Angina Group:Clinical diagnosis of unstable angina.
  • Sign informed consent.

Exclusion Criteria

  • Myocarditis, hypertrophic cardiomyopathy, ablation.
  • Malignant hypertension, severe arrhythmia.
  • Chronic muscle disorders, rhabdomyolysis.
  • Severe liver and kidney dysfunction.
  • Malignant tumors, acute cerebrovascular disease.
  • Severe neurosis, psychosis.
  • Patients who had any of the above were excluded.

Outcomes

Primary Outcomes

The change of cUck2 levels in AMI

Time Frame: It is totally 7 time points to detect cUck2, including the moment of admission, and the 1st day、the 2nd day、the 3th day、the 7th day、the 14th day、the 6th month after admission in AMI patients.

The investigators has found cUck2 has more close association with AMI.Detect cUck2 levels in different time points and it will give more information about its diagnostic value in AMI.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hong-Jin Wu

Clinical Professor

Beijing Haidian Hospital

Study Sites (1)

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