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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00201903
Other study ID # OCOG-2003-TFsubstudy
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated April 5, 2017
Start date January 2004
Est. completion date October 2006

Study information

Verified date May 2007
Source Ontario Clinical Oncology Group (OCOG)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To explore the relationship between tissue factor levels, tumour progression, activation of blood coagulation and venous thromboembolism with malignant glioma


Description:

To explore the relationship between tissue factor levels, tumour progression, activation of blood coagulation and venous thromboembolism with malignant glioma


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 2006
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- participation in PRODIGE

- adult patients

- newly diagnosed, biopsy-confirmed grade III/IV malignant gliomas

- undergone craniotomy or stereotactic biopsy > 2 days and < 4 weeks before

Exclusion Criteria:

- have known hereditary thrombophilia

- are receiving experimental antiangiogenic therapy

Study Design


Locations

Country Name City State
Canada Cross Cancer Institute Edmonton Alberta
Canada Princess Margaret Hospital Toronto Ontario
Canada Toronto-Sunnybrook Regional Cancer Centre Toronto Ontario
Canada CancerCare Manitoba Winnipeg Manitoba
United States Henry Ford Hospital Detroit Michigan
United States Huntsman Cancer Institute Salt Lake City Utah

Sponsors (2)

Lead Sponsor Collaborator
Ontario Clinical Oncology Group (OCOG) Ontario Cancer Research Network

Countries where clinical trial is conducted

United States,  Canada, 

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