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Clinical Trials/NCT02581618
NCT02581618
Completed
Not Applicable

Effect of One Cycle Remote Ischemic Preconditioning on Myocardial Injury After Percutaneous Coronary Interventions in Patients With Stable Coronary Artery Disease

Trakya University1 site in 1 country102 target enrollmentMay 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myocardial Ischemia
Sponsor
Trakya University
Enrollment
102
Locations
1
Primary Endpoint
hs-Troponin elevation
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Myocardial injury occurs after percutaneous coronary intervention due to micro emboli, ischemia-reperfusion injury or side branch occlusion. 3 cycles of ischemic preconditioning has been shown to be useful in preventing myocardial injury but it is not suitable to perform it especially in ad hoc interventions. In this study the investigators aim is to show whether one cycle remote ischemic preconditioning will be enough to prevent myocardial injury during percutaneous coronary intervention.

Detailed Description

About in one third of elective percutaneous coronary interventions (PCI) troponin release occurs showing myocardial necrosis. And it has been shown that myocardial necrosis due to coronary interventions has also adverse effects on long term prognosis. Beneficial effects of of ischemic preconditioning in elective PCI and in coronary artery bypass surgery has been shown in several studies. In most of the trials 3 cycles of ischemia was performed, but this is time consuming and it's not suitable to apply it, in ad-hoc interventions. The investigators found one study showing that one cycle will also be enough to prevent troponin elevation after elective PCI. The investigators aim was also to show that one cycle preconditioning performed just before coronary intervention will also be useful in preventing myocardial necrosis due to elective PCI.

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
February 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mustafa Adem YILMAZTEPE

Assistant Professor Of Medicine

Trakya University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Acute or chronic renal failure (Creatinin clearance \<60ml/dk)
  • Acute heart failure
  • Presence of hemodynamic instability
  • Left main interventions
  • Acute Coronary Syndrome
  • Patients in whom cuff inflation is contraindicated in upper extremities (fistula, lymphoedema etc)
  • Patients using nicorandil, glibenclamide or trimetazidine
  • Patients not accepting the study
  • Presence of troponin elevation before intervention
  • Presence or suspicion of pregnancy

Outcomes

Primary Outcomes

hs-Troponin elevation

Time Frame: after 16 hours

Study Sites (1)

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