Status:

COMPLETED

Pharmacological Postconditioning to Reduce Infarct Size Following Primary PCI

Lead Sponsor:

Rigshospitalet, Denmark

Collaborating Sponsors:

University Hospital, Gentofte, Copenhagen

Conditions:

Myocardial Infarction

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

Both pre- and postconditioning seem to protect cardiomyocytes during reperfusion therapy. Investigations both ex vivo and in vivo suggest that a gut derived hormone, Glucagon-Like-Peptide-1 (GLP-1), i...

Eligibility Criteria

Inclusion

  • More than 18 years of age.
  • STEMI less than 12 hours from onset of pain. STEMI defined as as ST-segment elevation in 2 contiguous electrocardiographic leads of \>0.1 mV in V4 - V6 or limb leads II, III and aVF, or \>0.2 mV in lead V1 - V3.
  • TIMI 0-1 in infarct related artery.
  • Oral and written informed consent.

Exclusion

  • Multivessel disease defined by one or more stenoses \>70% in diameter in the non infarct related artery.
  • Previous myocardial infarction.
  • Stent trombosis.
  • Previous CABG.
  • Less than TIMI 2 following wiring and predilatation of the infarct related artery but prior to postconditioning or placebo treatment.
  • Renal insufficiency (creatinin \>200).
  • Pregnancy or lactation.
  • Diabetic ketoacidose eller hypoglycemia (plasma glukose \< 2.5 mmol/l).
  • Pancreatitis.

Key Trial Info

Start Date :

January 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2015

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT00835848

Start Date

January 1 2009

End Date

May 1 2015

Last Update

May 5 2015

Active Locations (1)

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1

Heart Center, Rigshospitalet

Copenhagen, Denmark, 2100