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Treating Acute MI Patients With Aggrastat on Their Way to Hospital
This study is currently recruiting participants.
Verified by The Baruch Padeh Medical Center, Poriya, January 2009
First Received: March 1, 2006   Last Updated: January 18, 2009   History of Changes
Sponsored by: The Baruch Padeh Medical Center, Poriya
Information provided by: The Baruch Padeh Medical Center, Poriya
ClinicalTrials.gov Identifier: NCT00300833
  Purpose

Treating an AMI patient with ST elevation with Aggrastat in the ambulance on his or her way to the hospital.


Condition Intervention Phase
Acute Myocardial Infarction
Drug: Tirofiban
Phase IV

MedlinePlus related topics: Heart Attack
Drug Information available for: Tirofiban hydrochloride Tirofiban Tirofiban hydrochloride monohydrate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Efficacy Study

Further study details as provided by The Baruch Padeh Medical Center, Poriya:

Primary Outcome Measures:
  • mortality

Secondary Outcome Measures:
  • TIMI flow

Estimated Enrollment: 200
Study Start Date: January 2006
Intervention Details:
    Drug: Tirofiban
    pci
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00300833

Contacts
Contact: Yonathan Hasin, Professor 97246652648 yhasin@poria.health.gov.il

Locations
Israel
Cardiovascular Division, The Baruch Padeh Medical Center, Poriya, Recruiting
Tiberias, Israel, 15208
Magen David , Recruiting
Tiberias, Israel
Contact: Sergay Krablikov, Dr            
Sponsors and Collaborators
The Baruch Padeh Medical Center, Poriya
Investigators
Study Chair: Menachem Naheer The Baruch Padeh Medicel Center, Poriya, Tiberias, Israel
  More Information

No publications provided

Responsible Party: The baruch Padeh Medical center ( Menachem Nahir )
Study ID Numbers: Aggrastat in AMI.CTIL
Study First Received: March 1, 2006
Last Updated: January 18, 2009
ClinicalTrials.gov Identifier: NCT00300833     History of Changes
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Study placed in the following topic categories:
Necrosis
Heart Diseases
Tirofiban
Myocardial Ischemia
Vascular Diseases
Ischemia
Infarction
Myocardial Infarction

Additional relevant MeSH terms:
Necrosis
Heart Diseases
Pathologic Processes
Myocardial Ischemia
Vascular Diseases
Cardiovascular Diseases
Ischemia
Infarction
Myocardial Infarction

ClinicalTrials.gov processed this record on May 07, 2009