Evaluation of predelivery maternal fibrinogen as predictor for blood loss during childbirth
- Conditions
- coagulation and bleeding during labour and delivery, post partum haemorrhage (PPH)PPH in combination with fibrinogen concentration, parameters of plasmatic coagulation, factor XIII concentration and peripartum blood loss
- Registration Number
- DRKS00007873
- Lead Sponsor
- Charité Universitätsmedizin Berlin, Klinik für Geburtsmedizin, Campus Virchow-Klinikum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 1083
Inclusion Criteria
pregnant women at admission to the labour ward
- minimum age 18 years or parental permission
- consent of women for use of personal data
Exclusion Criteria
- not able to speak and understand german
- doubt of ability to judge
- elective caesarean delivery
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Prepartal determination of fibrinogen concentration (measured according to Clauss)<br><br>- peripartum measurement of blood loss systematically by a calibrated drape under buttocks while active bleeding (Brenner Medical, München) <br>
- Secondary Outcome Measures
Name Time Method - postpartum determination of fibrinogen concentration within 48 h