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NCT03522116 Clinical Trial

Relationship Between CMR-derived Parameters of Ischemia / Reperfusion Injury and Timing of CMR in STEMI

Myocardial Infarction Clinical Trial

Official title:
Relationship Between CMR-derived Parameters of Ischemia / Reperfusion Injury and the Timing of CMR After Reperfused ST-segment Elevation Myocardial Infarction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03522116
Other study ID # TimingReperfusionInjury
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2014
Est. completion date June 30, 2017

Study information
Verified date April 2018
Source Centre Hospitalier Universitaire Vaudois
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This a prospective observational study including patients with ST-segment elevation myocardial infarction undergoing cardiovascular magnetic resonance for clinical reason during the index hospitalization. This local registry stemmed from multi-center european registry on cardiovascular magnetic resonance

Recruitment information / eligibility
Status Completed
Enrollment 220
Est. completion date June 30, 2017
Est. primary completion date August 1, 2016
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of STEMI

- Undergoing CMR during the index hospitalization

Exclusion Criteria:

- Refractory cardiogenic shock

- claustrophobia

- eGFR<30 ml/min/1.73m2

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No intervention
No intervention

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Vaudois

Outcome
Type Measure Description Time frame Safety issue
Primary Metrics of ischemia / repercussion injury June 2017
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