Preoperative evaluation of bleeding risk during surgery
- Conditions
- ndiagnosed bleeding disorders (niet gediagnosticeerde stollingsstoornissen)Per operative blood loss (perioperatief bloedverlies)
- Registration Number
- NL-OMON26413
- Lead Sponsor
- Main investigator:Y. Henskens, ir., PhD. Maastricht Universitair Medisch Centrum (MUMC)
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 820
Inclusion Criteria
Adult subjects (at least 18 years of age) with planned elective surgery in:
oOrthopedic surgery
Exclusion Criteria
- Incapacitated subjects
- Patients < 18 years of age
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the validity of a diagnostic screening package for bleeding tendency consisting of point-of-care hemostatic tests and the ISTH-BAT, compared to the golden standard an haematologist currently uses for diagnosing bleeding disorders.
- Secondary Outcome Measures
Name Time Method 1. To develop a more efficient screening algorithm for patients with possible bleeding disorders.<br /><br>2. Describe differences in the usages of blood products and the hemoglobin drop per operatively between patients with bleeding symptoms and healthy controls (both preoperative patients).