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The Application of Comprehensive Prevention and Treatment Strategy of Placenta Accreta Spectrum Disorders

The Application of Comprehensive Prevention and Treatment Strategy of Placenta Accreta Spectrum Disorders

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06477497
Enrollment
33
Registered
2024-06-27
Start date
2024-07-01
Completion date
2025-11-30
Last updated
2024-06-27

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

Conditions

Placenta Accreta Spectrum

Keywords

placenta accreta spectrum disorders

Brief summary

Placenta accreta spectrum (PAS) disorders are pathological attachment of the placenta to myometrium, where trophoblastic cells invade the uterine placental interface. PAS can lead to severe postpartum hemorrhage or even maternal death. Prenatal diagnosis of PAS is essential for optimal obstetric management to improve the pregnancy outcomes. However, in some low resource regions in China, less than 20% PAS are detected before delivery. To explore the feasibility and universality of the bundled prevention and treatment strategy for placenta accreta spectrum disorders in different levels of medical institutions, and to investigate its effectiveness in improving the specialized disease management capabilities of medical institutions at all levels. We will conduct a regional, cluster-randomized trial to assess a multicomponent PAS management strategy to improve the prepartum detection rate of PAS.

Interventions

None listed

Sponsors

National Key Research and Development Program of China
CollaboratorUNKNOWN
Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women who have regular prenatal examination at the research hospitals * Pregnant women diagnosed with PAS before or after delivery

Exclusion criteria

* Pregnant women who have never been diagnosed with placental implantation disease throughout the pregnancy * Pregnant women who were lost to follow-up during the study period

Design outcomes

Primary

MeasureTime frame
antepartum diagnosis rate of PASthrough study completion, an average of 1.5 year

Contacts

Primary ContactJinsong Gao
gaojingsong@pumch.cn0861069156225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026