Evaluation of predelivery maternal fibrinogen as predictor for blood loss during childbirth

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00007873

Enrollment

1000

Registered

2015-03-13

Start date

2011-12-16

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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

Interventions

Group 1: women with vaginal delivery, prepartum fibrinogen level and peripartum blood loss

Eligibility

Sex/Gender

Female

Age

14 Years to No maximum

Inclusion criteria

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

Exclusion criteria: - not able to speak and understand german - doubt of ability to judge - elective caesarean delivery

Design outcomes

Primary

Measure	Time frame
- Prepartal determination of fibrinogen concentration (measured according to Clauss) - peripartum measurement of blood loss systematically by a calibrated drape under buttocks while active bleeding (Brenner Medical, München)	—

Secondary

Measure	Time frame
- postpartum determination of fibrinogen concentration within 48 h	—

Countries

Germany

Contacts

Public ContactChristian Bamberg

Charité Universitätsmedizin Berlin, Klinik für Geburtsmedizin, Campus Virchow-Klinikum

christian.bamberg@charite.de030-450 564 072

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026