Reperfusion Time in ST Segment Elevation Myocardial Infarction (STEMI)
Evaluation of a Fast Track for Patients With STEMI
1 other identifier
interventional
150
1 country
1
Brief Summary
Reperfusion delay in STEMI has been shown to be excessive in our community. In order to improve delay a fast track (direct transfer in catheterization laboratory) has been implemented. The present study aims at evaluating the benefits of this procedure.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2007
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2007
CompletedFirst Submitted
Initial submission to the registry
July 5, 2007
CompletedFirst Posted
Study publicly available on registry
July 6, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2007
CompletedAugust 20, 2008
August 1, 2008
9 months
July 5, 2007
August 19, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Door to balloon time
one year
Interventions
Eligibility Criteria
You may qualify if:
- Diagnosis of STEMI
You may not qualify if:
- On site resuscitated patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Geneva University Hospital, Emergency Service
Geneva, Canton of Geneva, 1211, Switzerland
Related Publications (1)
Grosgurin O, Plojoux J, Keller PF, Niquille M, N'koulou R, Mach F, Sarasin FP, Rutschmann OT. Prehospital emergency physician activation of interventional cardiology team reduces door-to-balloon time in ST-elevation myocardial infarction. Swiss Med Wkly. 2010 Apr 17;140(15-16):228-32. doi: 10.4414/smw.2010.12927.
PMID: 20131111DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Olivier Grosgurin, MD
University Hospital, Geneva
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 5, 2007
First Posted
July 6, 2007
Study Start
January 1, 2007
Primary Completion
October 1, 2007
Study Completion
October 1, 2007
Last Updated
August 20, 2008
Record last verified: 2008-08