Development of a perinatal trigger list for the detection of adverse events affecting mothers and their newborns in Germany

Development of a perinatal trigger list for the detection of adverse events affecting mothers and their newborns in Germany - ObsTT-A

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035566

Enrollment

Registered

2024-11-25

Start date

2024-12-09

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

Adverse events in obstetric care, including complications in mothers and newborns such as postpartum hemorrhage, infections, respiratory issues, or surgical risks.

Interventions

Group 1: Expert evaluation of potential triggers for adverse events in obstetric care through a Delphi survey.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: * Resident in Germany and German-speaking * Staff of inpatient obstetrics and healthcare facilities, including: 1. midwives/obstetricians 2. healthcare and paediatric nurses 3. physicians (gynaecologists) 4. paediatricians / neonatologists 5. quality and risk managers

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Consensus on a standardized list of triggers for the retrospective identification of adverse events in obstetric care.	—

Secondary

Measure	Time frame
Evaluation of the applicability of developed triggers in Germany.	—

Countries

Germany

Contacts

Public ContactMatthias Weigl

Institut für Patientensicherheit, Universitätsklinikum Bonn

matthias.weigl@ukbonn.de+49 228 287 10390

Outcome results

None listed

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