Clinical Trials Directory

Trials / Completed

CompletedNCT02830217

Evaluation of Soluble ST2 in Patients Receiving Primary PCI With ST-elevation Myocardial Infarction

Using Soluble ST2 to Predict Clinical Outcomes in Patients Receiving Primary Percutaneous Coronary Intervention With ST-elevation Myocardial Infarction

Status
Completed
Phase
Study type
Observational
Enrollment
200 (actual)
Sponsor
Wuhan Asia Heart Hospital · Academic / Other
Sex
All
Age
25 Years – 80 Years
Healthy volunteers
Not accepted

Summary

ST-elevation myocardial infarction (STEMI) is an urgent symptom associated with sudden myocardial ischemia and ST segment elevated in ECG. Primary percutaneous coronary intervention (PCI) re-open infarct artery efficiently for STEMI patients. However, patients are readmitted shortly after the primary PCI for several unfavorable clinical outcomes including thrombosis in stent, recurrence of myocardial infarction, stroke, and heart failure. This study is intended to test the predictive ability of a new biomarker soluble ST2 (sST2) in peripheral blood. Previous studies have shown that elevated sST2 is highly associated with unfavorable clinical outcomes of patients with ischemia heart diseases and heart failure. This study will further investigate the ability of sST2 to predict unfavorable outcomes for STEMI patients after primary PCI.

Conditions

Timeline

Start date
2015-12-01
Primary completion
2018-11-30
Completion
2018-12-20
First posted
2016-07-12
Last updated
2019-10-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02830217. Inclusion in this directory is not an endorsement.

Evaluation of Soluble ST2 in Patients Receiving Primary PCI With ST-elevation Myocardial Infarction (NCT02830217) · Clinical Trials Directory