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Analysis of clinical high-risk factors for severe postpartum hemorrhage of placenta previa: a retrospective study based on medical records

Analysis of clinical high-risk factors for severe postpartum hemorrhage of placenta previa

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035286
Enrollment
Unknown
Registered
2020-08-06
Start date
2020-08-04
Completion date
Unknown
Last updated
2020-08-10

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

Conditions

Placenta Accreta Spectrum

Interventions

case series:Nil

Sponsors

The First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: All the patients of placenta previa.

Exclusion criteria

Exclusion criteria: Pregnancy complications and complications such as hypertension, heart disease, and blood system diseases.

Design outcomes

Primary

MeasureTime frame
volume of blood loss;rate of hysterectomy;ICU admission;Neonatal asphyxia rate;—

Secondary

MeasureTime frame
clinical characteristics;—

Countries

China

Contacts

Public ContactGe Zhiping

The First Affiliated Hospital of Nanjing Medical University

gzp88142@163.com+86 13851528816

Outcome results

None listed

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