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Subrenal abdominal aortic balloon for dangerous placenta previa: a retrospective study

New ultrasound scoring system used to guide placement of abdominal aortic balloon: a retrospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044798
Enrollment
Unknown
Registered
2021-03-27
Start date
2021-04-26
Completion date
Unknown
Last updated
2021-10-26

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

Conditions

PAS

Interventions

abdominal aortic balloon placement group vs. non placement group:Nil

Sponsors

The First Affiliated Hospital, Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: We retrospectively analyzed the clinical data of PAS patients with placenta previa who underwent cesarean section from July 2019 to December 2020. The inclusion criteria were PAS patients with placenta previa diagnosed by color Doppler ultrasound and without other obstetric diseases.

Exclusion criteria

Exclusion criteria: PAS combined with placenta previa and undergoing emergency cesarean section.

Design outcomes

Primary

MeasureTime frame
intraoperative blood loss;red blood cell suspension infusion;blood transfusion rate;hysterectomy incidence; transfer to ICU rate;—

Countries

China

Contacts

Public ContactFusen Huang

The First Affiliated Hospital of Chongqing Medical University

793736612@qq.com+86 19923594184

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026