Reproducibility of Magnetic Resonance Myocardial Salvage Index - Tabular View

This Tabular View shows the required WHO registration data elements as marked by ^†

Descriptive Information Fields

Brief Title ^†

Reproducibility of Magnetic Resonance Myocardial Salvage Index

Official Title ^†

Reproducibility of Myocardial Salvage Index in Acute Myocardial Infarction by Cardiac Magnetic Resonance Imaging

Brief Summary

The myocardial salvage assessed by using multimodal cardiac magnetic resonance imaging is a rather new technique which can be used as a surrogate endpoint to reduce the sample size in studies comparing different reperfusion strategies in myocardial infarction. As reproducibility of myocardial salvage has not been evaluated appropriately, we aim to scan 20 patients on 2 subsequent days to evaluate reproducibility of myocardial salvage index.

Detailed Description

Study Phase

Study Type ^†

Observational

Study Design ^†

Cohort, Prospective

Primary Outcome Measure ^†

Myocardial salvage index reproducibility [ Time Frame: 2 days ] [ Designated as safety issue: No ]

Secondary Outcome Measure ^†

infarct size reproducibility [ Time Frame: 2 days ] [ Designated as safety issue: No ]
area at risk reproducibility [ Time Frame: 2 days ] [ Designated as safety issue: No ]
microvascular obstruction reproducibility [ Time Frame: 2 days ] [ Designated as safety issue: No ]

Condition ^†

Myocardial Infarction

Intervention ^†

Device: second magnetic resonance imaging scan

MEDLINE PMIDs

Links

Recruitment Information Fields

Recruitment Status ^†

Completed

Enrollment ^†

Start Date ^†

Completion Date

Eligibility Criteria ^†

Inclusion Criteria:

ST-elevation myocardial infarction
Primary percutaneous coronary intervention

Exclusion Criteria:

Contraindications for magnetic resonance imaging

Gender

Both

Ages

18 Years and older

Accepts Healthy Volunteers

Contacts ^††

Location Countries ^†

Germany

Administrative Information Fields

NCT ID ^†

NCT00794300

Organization ID

Repro100

Secondary IDs ^††

Study Sponsor ^†

University of Leipzig

Collaborators ^††

Investigators ^†

Principal Investigator:

Holger Thiele, MD

University of Leipzig

Information Provided By

University of Leipzig

Verification Date

November 2008

First Received Date ^†

November 19, 2008

Last Updated Date

November 19, 2008

^† Required WHO trial registration data element.
^†† WHO trial registration data element that is required only if it exists.