Analysis of the fibrinolytic potential during birth using point of care testing
- Conditions
- O72Postpartum haemorrhage
- Registration Number
- DRKS00021531
- Lead Sponsor
- Klinik für Anästhesiologie, Universitätsklinikum Heidelberg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
All patients, who give birth at the delivery ward of the gynecological clinic, University Hospital Heidelberg during the examination period and who consent to the implementation of this study, will be included. We want to include a total of 200 patients. Inclusion will take place in chronological order. The following criteria must be fulfilled:
written declaration of consent by the study participant,
Age> 18 years
Exclusion Criteria
Refusal to participate in the study,
Failing the inclusion criteria
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analysis of blood coagulation and the fibrinolytic potential using modern POC devices (TPA test) in different stages of delivery (blood collection before birth, 30 minutes after placental expulsion, 6 hours after birth)
- Secondary Outcome Measures
Name Time Method Comparison with clinical surrogate parameters: blood loss, rate of secondary haemorrhage, need for clinical interventions (e.g. uterotonic administration, balloon catheter insert, surgical or interventional care, etc.)