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Establishment of Evaluation for Diagnostic/Predictive Accuracy of Intraoperative Scoring System for PAS Severity

A novel scoring system for distinguishing the severity of Placenta Accreta Spectrum intraoperatively

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035266
Enrollment
Unknown
Registered
2020-08-05
Start date
2019-04-01
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:give scores

Sponsors

First Affiliated Hospital of Nanjing Medical University,
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Placenta previaThe was screened by doppler ultrasound examination at 20 weeks of gestation and reconfirmed to be PAS at 24-28 weeks. The imaging was done before delivery again to indicate the possibility of PAS.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
numbers of sever PAS;cases number of hysterectomy;massive postpartum hemorrhage;large usage of blood products;ICU admission;—

Countries

China

Contacts

Public ContactZHI-PING GE

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