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Fetal Loss in Women with Unprovoked Thromboembolism (FLUTE) - Article


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Clinical Trial: Fetal Loss in Women with Unprovoked Thromboembolism (FLUTE)

This study is not yet open for patient recruitment.
Verified by McMaster University September 2005

Sponsors and Collaborators: McMaster University
Canadian Institutes of Health Research
Information provided by: McMaster University
ClinicalTrials.gov Identifier: NCT00149357

Purpose

To determine the risk of fetal loss in women with unprovoked venous thromboembolism (VTE) who do not have identifiable inherited thrombophilia compared with women who have the diagnosis of VTE excluded.
Condition
Venous Thromboembolism
fetal loss

MedlinePlus related topics:  Vascular Diseases

Study Type: Observational
Study Design: Natural History, Cross-Sectional, Defined Population, Retrospective/Prospective Study

Official Title: Determining the Risk of Fetal Loss in Women with Unprovoked Venous Thromboembolism (VTE) Who Do NOT Have Identifiable Inherited Thrombophilia Compared with Women Who Have the Diagnosis of VTE Excluded

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Female
  • At least 18 years of age
  • Symptomatic for unprovoked venous thromboembolism (DVT or PE)
  • At least one pregnancy not terminated intentionally

Exclusion Criteria:

  • Previous VTE in patients with current VTE excluded

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00149357

Lorraine Weise-Kelly, Ph.D.      905-527-2299  Ext. 43772    kellyla@mcmaster.ca
Anita Polgar      905-527-2299  Ext. 42648    polgara@mcmaster.ca

Canada, Ontario
      McMaster University Medical Centre, Hamilton,  Ontario,  L8N 3Z5,  Canada
Huyen Tran, M.D.  905-521-2100  Ext. 73928    tranha@mcmaster.ca 
Huyen Tran, M.D.,  Principal Investigator

      Henderson Research Centre, Hamilton,  Ontario,  L8V 1C3,  Canada
Clive Kearon, M.D.  905-527-2299  Ext. 42419    kearonc@mcmaster.ca 
Clive Kearon, M.D.,  Principal Investigator

      Hamilton General Hospital, Hamilton,  Ontario,  L8L 2X2,  Canada
Schulman Sam, M.D.  905-527-4322  Ext. 44479    schulms@mcmaster.ca 
Sam Schulman, M.D.,  Principal Investigator

      St. Joseph''''s Hospital, Hamilton,  Ontario,  L8N 4A6,  Canada
Mark Crowther, M.D.  905-521-6024    crowthrm@mcmaster.ca 
Mark Crowther, M.D.,  Principal Investigator

Study chairs or principal investigators

Huyen Tran, M.D.,  Study Chair,  McMaster University; Department of Medicine   
Jeffrey Ginsberg, M.D.,  Principal Investigator,  McMaster University; Department of Medicine   
Clive Kearon, M.D.,  Principal Investigator,  McMaster University; Department of Medicine   
Jim Julian, M.Math,  Principal Investigator,  McMaster University; Dept. of Clinical Epidemiology & Biostatistics   
Val Mueller, M.D.,  Principal Investigator,  McMaster University; Division of Obstetrics and Gynecology   

More Information

Study ID Numbers:  CTMG-2005-FLUTE
Last Updated:  September 7, 2005
Record first received:  September 6, 2005
ClinicalTrials.gov Identifier:  NCT00149357
Health Authority: Canada: Health Canada
ClinicalTrials.gov processed this record on 2005-09-13

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December 4, 2008



Page Updated: September 6, 2005
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