Clinical Trials Directory

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UnknownNCT02295150

Prophylaxis of Venous Thromboembolism After Bariatric Surgery

Prospective, Pharmacokinetic Study for Determination of the Relationship Between Lean Body Weight and Anti-Xa Activity 4 Hours After Subcutaneous Injection of 5700 IU Nadroparin in Morbidly Obese Patients After Bariatric Surgery.

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Rijnstate Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGNadroparinPatients receive before surgery 3 days 2850 IU nadroparin. anti-Xa levels will be measured. After surgery they receive 5700 IU for 4 weeks as standard care in our hospital. 3 days and 4 weeks after surgery anti-Xa levels will be measured again.

Timeline

Start date
2013-03-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2014-11-20
Last updated
2014-11-20

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02295150. Inclusion in this directory is not an endorsement.