Back to resultsTreating Acute MI Patients With Aggrastat on Their Way to Hospital
Primary Purpose
Acute Myocardial Infarction
Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Tirofiban
Sponsored by
About this trial
This is an interventional treatment trial for Acute Myocardial Infarction
Eligibility Criteria
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
Sites / Locations
- Cardiovascular Division, The Baruch Padeh Medical Center, Poriya,Recruiting
- Magen David ,Recruiting
Outcomes
Primary Outcome Measures
mortality
Secondary Outcome Measures
TIMI flow
feeling better
Full Information
NCT ID
NCT00300833
First Posted
March 1, 2006
Last Updated
August 10, 2011
Sponsor
The Baruch Padeh Medical Center, Poriya
1. Study Identification
Unique Protocol Identification Number
NCT00300833
Brief Title
Treating Acute MI Patients With Aggrastat on Their Way to Hospital
Study Type
Interventional
2. Study Status
Record Verification Date
January 2009
Overall Recruitment Status
Unknown status
Study Start Date
January 2006 (undefined)
Primary Completion Date
January 2012 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
The Baruch Padeh Medical Center, Poriya
4. Oversight
5. Study Description
Brief Summary
Treating an AMI patient with ST elevation with Aggrastat in the ambulance on his or her way to the hospital.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myocardial Infarction
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Tirofiban
Intervention Description
pci
Primary Outcome Measure Information:
Title
mortality
Time Frame
immidiately
Secondary Outcome Measure Information:
Title
TIMI flow
Description
feeling better
Time Frame
24 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yonathan Hasin, Professor
Phone
97246652648
Email
yhasin@poria.health.gov.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Menachem Naheer
Organizational Affiliation
The Baruch Padeh Medicel Center, Poriya, Tiberias, Israel
Official's Role
Study Chair
Facility Information:
Facility Name
Cardiovascular Division, The Baruch Padeh Medical Center, Poriya,
City
Tiberias
ZIP/Postal Code
15208
Country
Israel
Individual Site Status
Recruiting
Facility Name
Magen David ,
City
Tiberias
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sergay Krablikov, Dr
12. IPD Sharing Statement
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Treating Acute MI Patients With Aggrastat on Their Way to Hospital
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