Fetal Loss in Women With Unprovoked Thromboembolism (FLUTE)

McMaster University

Status: Terminated

Conditions: Venous Thromboembolism; Fetal Death

Treatments: Other: Thrombophilia Testing

Study type: Observational

Funder types: Other

Identifiers

NCT00149357

CTMG-2005-FLUTE

Details and patient eligibility

About

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.

Enrollment: 239 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Female
• At least 18 years of age
• Symptomatic for unprovoked venous thromboembolism (deep vein thrombosis [DVT] or pulmonary embolism [PE])
• At least one pregnancy not terminated intentionally

Exclusion criteria

• Previous VTE in patients with current VTE excluded

Trial design

239 participants in 1 patient group

1, 2 ,3

Description:

Group 1 Women with unprovoked VTE and No Known Thrombophilia Group 2 Women who are investigated for VTE and are negative (Control) Group 3 Women with unprovoked VTE who have Thrombophilia

Treatment:

Other: Thrombophilia Testing