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Clinical Trials/NCT02767960
NCT02767960CompletedNot Applicable

Change of Serum Tenascin-C Concentration and the Relationship With Hs-CRP,cTnI and Prognosis in Patients With Acute Coronary Syndrome

The First Affiliated Hospital of Dalian Medical University1 site in 1 country183 target enrollmentStarted: May 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
183
Locations
1
Primary Endpoint
Serum Tenascin-C concentration

Study Overview

Brief Summary

This study valuates the serum Tenascin-C concentration in patients with acute coronary syndrome.

Detailed Description

It is found that Tenascin-C plays an important role in ventricular remodeling, heart failure, aortic dissection, rheumatic heart disease and other cardiovascular diseases, which may be a new marker for the diagnosis and prognosis prediction of these diseases. However, there is few relevant studies about the Tenascin-C concentration in patients with acute coronary syndrome.This study valuates the serum Tenascin-C concentration in patients with acute coronary syndrome.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • .diagnosed as acute coronary syndrome,including STEMI,non-STEMI,and UAP.
  • with left ventricular ejection fraction(LVEF)>=45%
  • written informed consents are obtained
  • admitted within 24 hours after chest pain attacked

Exclusion Criteria

  • complicated with rheumatic heart disease, coronary arteritis, hypertrophic cardiomyopathy or dilated cardiomyopathy
  • complicated with malignant tumor,the immune system diseases, blood system diseases, recently (within 2 weeks) taking glucocorticoid drugs, the use of immunosuppressive agents and cerebral infarction
  • with acute or chronic infection, surgery or trauma in the last month
  • secondary hypertension, severe liver dysfunction,severe renal insufficiency
  • with abnormal thyroid function or allergy to iodine agent
  • refusal to sign the informed consent

Outcomes

Primary Outcomes

Serum Tenascin-C concentration

Time Frame: 12 months

Serum Tenascin-C concentration in ng/ml

Secondary Outcomes

  • Relationship between Tenascin-C and high sensitive C reaction protein (hs-CRP) concentration(12 months)
  • Relationship between Tenascin-C and Troponin-I (Tn-I) concentration(12 months)
  • MACEs during 12-month follow-up(12 months)

Investigators

Sponsor
The First Affiliated Hospital of Dalian Medical University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rchuang

Professor

The First Affiliated Hospital of Dalian Medical University

Study Sites (1)

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