An open, randomised, single center study to compare a low suction intra and postoperative autologous blood transfusion system with no drainsystem at all with regards to haemoglobin loss following primary total hip arthroplasty implantatio
Completed
- Conditions
- hip replacement operationtotal hip arthroplasty10023213
- Registration Number
- NL-OMON32927
- Lead Sponsor
- Isala Klinieken
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 214
Inclusion Criteria
age 18 years and up
provision of written informed consent
the patient is subject to a total hip arthroplasty implantation
Exclusion Criteria
coagulation disorders, including thrombo embolic history
malignancy
ongoing infections
untreated hypertension
renal dysfunction
unstable angina pectoris
myocardial infarction within the past 12 months
bypass-operation within the past 12 months
intake of anticoagulants
participation in other clinical trials dealing with any drugs which influences blood loss
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>for summary see the dutch version above</p><br>
- Secondary Outcome Measures
Name Time Method <p>for summary see the dutch version above</p><br>