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Clinical Trials/NCT01906918
NCT01906918
Unknown
Not Applicable

Evaluation of Remote Preconditioning on Heart Resistance to Ischemia and Reperfusion Injury

University of Campinas, Brazil1 site in 1 country120 target enrollmentAugust 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
University of Campinas, Brazil
Enrollment
120
Locations
1
Primary Endpoint
Molecular pathway activation
Last Updated
12 years ago

Overview

Brief Summary

Strategies for myocardial protection during open heart surgeries are desired. Several experimental studies have shown beneficial effects of remote ischemic preconditioning (RIPC). The underlying mechanisms are not totally understood. This study intends to evaluate molecular mechanisms involved with RIPC on myocardium of patients underwent open heart surgeries.

Registry
clinicaltrials.gov
Start Date
August 2013
End Date
August 2015
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Campinas, Brazil
Responsible Party
Principal Investigator
Principal Investigator

Orlando Petrucci

Phd

University of Campinas, Brazil

Eligibility Criteria

Inclusion Criteria

  • Patients older than 18 years
  • Scheduled for coronary artery bypass grafting with or without valve replacement associated
  • Use of blood cardioplegia
  • EuroSCORE II greater than or equal to 1.0%

Exclusion Criteria

  • History of cardiogenic shock
  • Complications in the admission
  • Pregnant patients
  • Severe peripheral arterial disease affecting the upper limbs
  • Liver failure (bilirubin ˃ 20 mmol / L, INR 2.0 ˃)
  • Significant pulmonary disease (˂ FEV1 40%)
  • Renal failure with glomerular filtration rate ˂ ml/min/1,73 m²
  • Concomitant treatment with glibenclamide or nicorandil (medications that interfere with cardioprotection induced by IPCR)

Outcomes

Primary Outcomes

Molecular pathway activation

Time Frame: 2 days

Inflammatory response

Time Frame: 10 days

Secondary Outcomes

  • All cause of mortality(180 days)

Study Sites (1)

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