Prophylaxis of Venous Thromboembolism After Bariatric Surgery

Status Recruiting

Clinical Trial Summary

This study is a prospective evaluation of the relationship between lean body weight and anti-Xa activity and 5700 International Units (IU) nadroparin 4 hours after subcutaneous administration in morbidly obese patients after bariatric surgery.

Clinical Trial Description

There is no guideline for postoperative thromboembolic prevention in morbidly obese patients.

The investigators goal is to examine which dose of nadroparin is effective. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02295150
Study type	Interventional
Source	Rijnstate Hospital
Contact	Wendy Schijns, MD
Phone	+31 88 005 8888
Email	wschijns@rijnstate.nl
Status	Recruiting
Phase	Phase 4
Start date	March 2013
Completion date	June 2015

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