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Clinical Trial Summary

The purpose of this study is to evaluate the potential diagnostic and prognosis value of circulating microRNAs compared with cTnI for suspected ACS patients at the emergency department (ED) and intensive care unit (ICU).


Clinical Trial Description

The present study is a single-center, prospective diagnostic study among patients presenting to the ED or ICU within 24 h of onset of chest pain suggestive of suspected ACS.

We propose to construct the biobank of ACS and evaluate the potential diagnostic value of circulating microRNAs compared with cTnI for suspected ACS patients. All the patients are to be followed up for 6 months. Final diagnosis was made by an expert panel cardiologist, based on all available clinical information including cTnI measurements, ECG, coronary angiography, cardiac exercise tests and information from hospital discharge letters.

The concentrations of microRNAs will be evaluated by quantitative reverse transcription PCR, using highly specific primers and hybridization probes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02755207
Study type Observational
Source Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Contact bin he
Email hebinicu@139.com
Status Recruiting
Phase
Start date April 2016
Completion date December 2020

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