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Efficacy of Prophylactic Internal Iliac Artery Balloon Catheterization in the Management of Placenta Previa and Accreta

the Efficacy of Prophylactic Internal Iliac Artery Balloon Catheterization in the Management of Placenta Previa and Accreta

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02966197
Enrollment
114
Registered
2016-11-17
Start date
2015-06-30
Completion date
2016-09-30
Last updated
2016-11-17

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

Conditions

Placenta Accreta, Placenta Previa

Brief summary

Placenta previa and accreta both could potentially cause serious postpartum hemorrhage and even maternal death. Interventional radiological techniques have been developed to limit massive hemorrhage during caesarean section. This study investigated the efficacy of prophylactic internal iliac artery balloon catheterization in management for placenta previa and accreta.

Detailed description

Placenta previa and accreta both could potentially cause serious postpartum hemorrhage and even maternal death. Interventional radiological techniques have been developed to limit massive hemorrhage during caesarean section. This study investigated the efficacy of prophylactic internal iliac artery balloon catheterization in management for placenta previa and accreta. Between June 2015 and August 2016,patients were personally recruited and managed by the authors,and assigned to either balloon group or control group by their willingness to catheterization or not. Both groups benefitted similar management protocol with the exception of interventional radiology operation. Intraoperative blood loss, transfusion volume, radiation dose, exposure time, surgical duration, procedure complications and neonatal outcomes were analyzed.

Interventions

PROCEDUREprophylactic internal iliac artery balloon catheterization

Between June 2015 and August 2016

DEVICEProphylactic internal iliac artery balloon
RADIATIONRadiology operation

Sponsors

Deng Dongrui
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Pregnant women were eligible if they were diagnosed to have placenta previa and accreta by sonographic examination or Magnetic Resonance Imaging.

Exclusion criteria

* Any case who had bleeding disorder or underwent emergency cesarean delivery was excluded.

Design outcomes

Primary

MeasureTime frame
blood lossintraoperative

Secondary

MeasureTime frame
operation durationintraoperative
fluid transfusionintraoperative
blood transfusionintraoperative

Outcome results

None listed

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