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Clinical Trials/JPRN-UMIN000006543
JPRN-UMIN000006543Completed未知

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

Kansai Medical University Hirakata hospital0 sites100 target enrollmentStarted: December 31, 2013Last updated:

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18years-old to 90years-old (—)
Sex
All

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.

Investigators

Sponsor
Kansai Medical University Hirakata hospital

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