Special Drug Use Investigation for ARIXTRA (Fondaparinux) Abdominal (Urology,Obstetrics,Gynecology)

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

475 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-12-31

Study Completion Date

2013-10-31

Brief Summary

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The purpose of this study is to collect and assess information on safety and efficacy of fondaparinux in patients undergoing abdominal surgery in urology, obstetrics and gynecology departments who are at high risk of venous thromboembolism.

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Detailed Description

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Conditions

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Cardiovascular Disease

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Patients prescribed fondaparinux

Patients undergoing abdominal surgery in urology, obstetrics and gynecology departments prescribed fondaparinux during study period

Fondaparinux Sodium

Intervention Type DRUG

Interventions

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Fondaparinux Sodium

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing abdominal surgery in urology, obstetrics and gynecology departments

Exclusion Criteria

* Patients with a history of hypersensitivity to the ingredients of fondaparinux
* Patients with bleeding (bleeding in important organs, sucn as retroperitoneal bleed)
* Patients with acute bacterial endocarditis
* Patients with severe renal impairment

Eligible Sex

ALL

Accepts Healthy Volunteers

No