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Female Sex is an Independent Predictor of Death and Bleeding Among Fibrinolytic Treated Patients With AMI
This study has been completed.

First Received on October 27, 2005.   No Changes Posted
Sponsor: New York University School of Medicine
Collaborators: The Cleveland Clinic
Centocor, Inc.
Eli Lilly and Company
Information provided by: New York University School of Medicine
ClinicalTrials.gov Identifier: NCT00245648
  Purpose

This study evaluated differences between men and women in the presentation, management and outcome of heart attacks within the GUSTO V study.


Condition Intervention Phase
Myocardial Infarcton
Drug: fibrinolytic therapy or combination reduced fibrinolytic therapy
Phase III

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Female Sex is an Independent Predictor of Death and Bleeding Among Fibrinolytic Treated Patients With AMI; Results of the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries - V Trial

Further study details as provided by New York University School of Medicine:

Detailed Description:

The Global Use of Strategies to Open Occluded Arteries in Acute Coronary Syndromes (GUSTO) V trial examined a large, contemporary cohort of women and men with ST elevation myocardial infarction (STEMI) treated with fibrinolytic therapy. The objective of the present study was to evaluate sex differences in presentation, management and outcome in GUSTO V.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • inclusion into GUSTO V

Exclusion Criteria:

  • lack of availability of data (database study)
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00245648

Locations
United States, New York
NYU School of Medicine
New York, New York, United States, 10016
Sponsors and Collaborators
New York University School of Medicine
The Cleveland Clinic
Centocor, Inc.
Eli Lilly and Company
Investigators
Principal Investigator: Harmony Reynolds NYU School of Medicine
  More Information

Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00245648     History of Changes
Other Study ID Numbers: GUSTOVsex
Study First Received: October 27, 2005
Last Updated: October 27, 2005
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Hemorrhage
Pathologic Processes
Tissue Plasminogen Activator
Fibrinolytic Agents
Fibrin Modulating Agents
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Cardiovascular Agents
Therapeutic Uses
Hematologic Agents

ClinicalTrials.gov processed this record on February 12, 2012