Evaluation of Plasma Non-coding RNAs as Biomarkers in Coronary Heart Disease

T

Tongji Hospital

Status

Invitation-only

Conditions

Coronary Disease

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02751060
TJ-IRB20160305

Details and patient eligibility

About

The purpose of this study is to determine whether the expression level of miR-320a are effective as biomarker in evaluating the diagnosis, prognosis and treatment effects of coronary heart disease.

Enrollment

4,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older;
  • the most recent symptoms of coronary heart disease within 7 days;
  • meet one of the following conditions: A. clinical history of typical ischemic chest pain (more than 5 minutes of persistent chest pain); B. serum cardiac biomarkers positive (TnT/I or creatine kinase peak greater than 99% of URL); C. Electrocardiogram changes of myocardial ischemia.

Exclusion criteria

  • pregnant women or plan to;
  • participate in any drug clinical trials within 3 months;
  • patients with life-threatening complications, or the researchers determined that the survival time of patients with no more than 1 years;
  • serious neurological disease (Alzheimer's disease, Parkinson syndrome, progressive lower limbs or deaf patients);
  • previous history of cancer or tumor, or pathological examination confirmed precancerous lesions (such as breast ductal carcinoma in situ, or atypical hyperplasia of the cervix);
  • patients refused to comply with the requirements of this study to complete the research work;
  • according to the researchers, patients can not complete the study or not to comply with the requirements of this study (because of the reasons for the management or other reasons).

Trial design

4,000 participants in 1 patient group

patients with coronary heart disease symptoms
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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