Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Nadroparin | Patients 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.