Viewing Study NCT00149357


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Study NCT ID: NCT00149357
Status: TERMINATED
Last Update Posted: 2017-03-23
First Post: 2005-09-06
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Fetal Loss in Women With Unprovoked Thromboembolism (FLUTE)
Sponsor: McMaster University
Organization:

Study Overview

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
Status: TERMINATED
Status Verified Date: 2017-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Funding withdrawn due to low enrollment
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is 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 venous thromboembolism (VTE) excluded.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: