Treating Acute MI Patients With Aggrastat on Their Way to Hospital
Sponsor
The Baruch Padeh Medical Center, Poriya (Other)
Overall Status
Unknown status
CT.gov ID
NCT00300833
Collaborator
(none)
200
2
100
Study Details
Study Description
Brief Summary
Treating an AMI patient with ST elevation with Aggrastat in the ambulance on his or her way to the hospital.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 4 |
Study Design
Study Type:
Interventional
Anticipated Enrollment
:
200 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Study Start Date
:
Jan 1, 2006
Anticipated Primary Completion Date
:
Jan 1, 2012
Outcome Measures
Primary Outcome Measures
- mortality [immidiately]
Secondary Outcome Measures
- TIMI flow [24 hours]
feeling better
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
patients with acute Myocardial infarction with ST elevation , and moving by ambulance to Poriya hospital
Exclusion Criteria:
- women less than 50 years old and 80 years old, bleeding tendency, stroke in the past
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Cardiovascular Division, The Baruch Padeh Medical Center, Poriya, | Tiberias | Israel | 15208 | |
| 2 | Magen David , | Tiberias | Israel |
Sponsors and Collaborators
- The Baruch Padeh Medical Center, Poriya
Investigators
- Study Chair: Menachem Naheer, The Baruch Padeh Medicel Center, Poriya, Tiberias, Israel
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00300833
Other Study ID Numbers:
- Aggrastat in AMI.CTIL
First Posted:
Mar 10, 2006
Last Update Posted:
Aug 11, 2011
Last Verified:
Jan 1, 2009