Skip to main content
Clinical Trials/CTRI/2019/06/019599
CTRI/2019/06/019599
Active, not recruiting
未知

Perioperative Major Adverse Cardiac Events in high risk patients undergoing major non cardiac surgeries: how accurately does pro-BNP and cardiac Troponin T predict the occurrence of major adverse cardiac events?

Postgraduate Institute of Medical Education and Research Chandigarh0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Postgraduate Institute of Medical Education and Research Chandigarh
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational

Investigators

Sponsor
Postgraduate Institute of Medical Education and Research Chandigarh

Eligibility Criteria

Inclusion Criteria

  • Patients with prior history of coronary artery disease will be defined as having any one of the following:
  • i)Definite CAD as indicated by a previous history of MI, typical angina or ECG changes suggestive of previous MI without a documented history of MI
  • ii)Patient who underwent coronary artery reperfusion therapy including previous fibrinolytic therapy, percutaneous coronary intervention and coronary angioplasty.
  • Patient at risk of coronary artery disease will be defined as those with age 45 yr or older and had at least one of the following major cardiac risk factors34:
  • 1\) Diabetes mellitus
  • 2\) Peripheral artery disease (i.e. intermittent claudication or history of vascular surgery except arteriovenous shunt and vein\-stripping procedures)
  • 3\) History of hospitalization for congestive heart failure
  • 4\) Renal insufficiency (defined as preoperative creatinine \>150 µmol litre\-1\)
  • 5\) History of cerebral vascular event
  • 6\) Aortic valve stenosis (defined as aortic valve area \<1 cm2\)

Exclusion Criteria

  • Patients will be excluded from study participation if they had no signed informed consent.

Outcomes

Primary Outcomes

Not specified

Similar Trials