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Bilateral internal iliac artery balloon occlusion for the management of pernicious placenta previa and accreta

Bilateral internal iliac artery balloon occlusion for the management of pernicious placenta previa and accreta

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012244
Enrollment
Unknown
Registered
2017-08-04
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

pernicious placenta previa and accreta

Interventions

trial group:bilateral internal iliac artery occlusion in cesarean section
control group:conditional management

Sponsors

West China Second University Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. pernicious placenta previa; 2. placenta accreta diagnosed by ultrasound or MRI; 3. singleton; 4. gestational age =28 weeks; 5. agree to join this study.

Exclusion criteria

Exclusion criteria: 1. twin pregnancy; 2. deny to join this study.

Design outcomes

Primary

MeasureTime frame
RBC transfusion;—

Secondary

MeasureTime frame
estimated blood loss;—

Countries

China

Contacts

Public ContactXinghui Liu

West China Second University Hospital of Sichuan University

xinghuiliu@163.com+86 13881883798

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026