- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00300833
Treating Acute MI Patients With Aggrastat on Their Way to Hospital
August 10, 2011 updated by: The Baruch Padeh Medical Center, Poriya
Treating an AMI patient with ST elevation with Aggrastat in the ambulance on his or her way to the hospital.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
200
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yonathan Hasin, Professor
- Phone Number: 97246652648
- Email: yhasin@poria.health.gov.il
Study Locations
-
-
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Tiberias, Israel, 15208
- Recruiting
- Cardiovascular Division, The Baruch Padeh Medical Center, Poriya,
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Tiberias, Israel
- Recruiting
- Magen David ,
-
Contact:
- Sergay Krablikov, Dr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
mortality
Time Frame: immidiately
|
immidiately
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
TIMI flow
Time Frame: 24 hours
|
feeling better
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Menachem Naheer, The Baruch Padeh Medicel Center, Poriya, Tiberias, Israel
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2006
Primary Completion (Anticipated)
January 1, 2012
Study Registration Dates
First Submitted
March 1, 2006
First Submitted That Met QC Criteria
March 9, 2006
First Posted (Estimate)
March 10, 2006
Study Record Updates
Last Update Posted (Estimate)
August 11, 2011
Last Update Submitted That Met QC Criteria
August 10, 2011
Last Verified
January 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Aggrastat in AMI.CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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