A prospective cohort study of postpartum hemorrhage prediction

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200063094

Enrollment

Unknown

Registered

2022-08-30

Start date

2022-08-31

Completion date

Unknown

Last updated

2023-04-12

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

Conditions

Postpartum hemorrhage

Interventions

None listed

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women aged 18-55 years who plan to have regular obstetrics and give birth in this unit.

Exclusion criteria

Exclusion criteria: Women who do not receive informed consent.

Design outcomes

Primary

Measure	Time frame
Postpartum hemorrhage;	—

Countries

China

Contacts

Public ContactXu Chen

Tianjin Central Hospital of Obstetrics and Gynecology

chenxu2665@126.com+86 18920196555

Outcome results