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Efficacy and safety of Fondaparinux for prevention of venous thromboembolism (VTE) after abdominal surgery

Not Applicable
Conditions
Colorectal cancer patients performed laparoscopic surgery at high risk of VTE
Registration Number
JPRN-UMIN000006543
Lead Sponsor
Kansai Medical University Hirakata hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patient who meet contraindication or precaution in package insert of anticoagulants such as Fondaparinux, UFH, LMWH, and Danaparoid 2.Patient who have experience of lower limb orthopedic surgery, abdominal surgery, cardiovascular surgery within 3 month of enrollment 3.Patient who receive contra indicated concomitant drug within 1 week after Fondaparinux administration. 4.VTE patient diagnosed before surgery 5.Patient whose D-dimer above 1 micro gram before surgery 6.Patient who have history of arterial thromboembolism 7.Drug addiction or alcohol abuse. 8.Patient who scheduled other surgery during the study 9.Pregnant women or women who have possibility of pregnancy. 10.Patient who judged inadequate to join the study by the doctor in charge.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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