Predictors of Bleeding Evaluation in Adult Hematologic Patients with Bleeding Tendencies Patients with established bleeding disorders: The BePa verification study
Recruiting
- Conditions
- hemorrhagic diathesisbleeding disorder1006447710005330
- Registration Number
- NL-OMON53063
- Lead Sponsor
- Medisch Universitair Ziekenhuis Maastricht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 140
Inclusion Criteria
Age => 18 years
Signed informed consent
Exclusion Criteria
Pregnancy (or lactating);
Active bleeding due to medical interventions or surgical/obstetrical causes
Use of any interfering medicatie < 48 hours before laboratory testing
Known platelet level lower than 100,000/µl
Known hematocrit lower than 30%
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method