Optimizing anti coagulant therapy in neurosurgical interventions in patients with an increased risk for thrombo-embolic complications.
Recruiting
- Conditions
- abnormal blood clottingvasculair illness1000972010014523
- Registration Number
- NL-OMON55381
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 280
Inclusion Criteria
Intracranial, tumour or trauma surgery,
>180 min estimates surgical intervention time
>240 min time under anaesthesia
Exclusion Criteria
Age under 18 years
Perioperative continuation of anti coagulant therapy indicated other than
prophylactic low molecular weight heparin
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary goal of the current study is to investigate whether the combination<br /><br>of perioperative intermittent pneumatic compression and LMWH has a lower<br /><br>incidence of postoperative thrombo-embolic complications within a week after a<br /><br>high risk neurosurgical intervention in comparison to patients receiving merely<br /><br>LMWH prophylaxis.</p><br>
- Secondary Outcome Measures
Name Time Method