CMR Repeatability in STEMI

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Elisa McAlindon, University of Bristol
ClinicalTrials.gov Identifier:
NCT01468662
First received: November 7, 2011
Last updated: July 8, 2013
Last verified: July 2013

November 7, 2011
July 8, 2013
November 2011
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Complete list of historical versions of study NCT01468662 on ClinicalTrials.gov Archive Site
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CMR Repeatability in STEMI
Cardiovascular Magnetic Resonance Scan Repeatability in ST Segment Elevation Myocardial Infarction

The investigators propose to conduct a study to measure the reproducibility of CMR parameters that have been used to predict outcome following PPCI: infarct size, left ventricular volumes, myocardial salvage, microvascular obstruction (MVO) and myocardial oedema.

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Observational
Observational Model: Case-Only
Time Perspective: Prospective
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Probability Sample

ST segment elevation myocardial infarction

STEMI
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STEMI
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
40
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Inclusion Criteria:

Participant may enter study if ALL of the following apply

  1. ST segment myocardial infarction as defined by ECG (by 2 contiguous limb leads with >1 mm ST-segment elevation, or >2 mm ST-segment elevation in contiguous precordial leads, or new LBBB) and > 20 minutes of cardiac chest pain
  2. Written informed consent

Exclusion Criteria:

Participant may not enter study if ANY of the following apply

  1. Contraindication to MRI (implanted pacemaker/ defibrillator, ferromagnetic metal implant/ injury, claustrophobia, obesity/ too large for CMR scanner)
  2. Known allergy to gadolinium
  3. Chronic atrial fibrillation
  4. Renal impairment with eGFR <30
  5. Cardiogenic shock
  6. Patients with special communication needs
Female
18 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
United Kingdom
 
NCT01468662
Study 1569
No
Elisa McAlindon, University of Bristol
University of Bristol
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Principal Investigator: Elisa McAlindon, BMBS University of Bristol
University of Bristol
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP