Analysis of the fibrinolytic potential during birth using point of care testing

Analysis of the fibrinolytic potential during birth using point of care testing - FYPPREG-Trial (Fibrinolytic Potential in Pregnancy -Trial)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00021531

Enrollment

200

Registered

2020-05-07

Start date

2020-05-15

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

O72

Interventions

Group 1: Analysis of the fibrinolytic potential during childbirth via point-of-care testing of blood samples at three different times (shortly before birth, 30 minutes after placental expulsion, 6 hou

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria: Refusal to participate in the study, Failing the inclusion criteria

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
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.)	—

Countries

Germany

Contacts

Public ContactFelix Schmitt

Klinik für Anästhesiologie, Universitätsklinikum Heidelberg

felix.schmitt@med.uni-heidelberg.de00 49 6221 56 39421

Outcome results

None listed

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