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The abdominal aorta balloon occlusion for the prevention of haemorrhage during caesarean section in parturients with placenta accreta: A Randomized Controlled Trial

The abdominal aorta balloon occlusion for the prevention of haemorrhage during caesarean section in parturients with placenta accreta: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008842
Enrollment
Unknown
Registered
2016-07-14
Start date
2016-07-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

haemorrhage during caesarean section in parturients with placenta accreta

Interventions

abdominal aorta balloon group:abdominal aorta balloon
traditional management group:traditional management

Sponsors

First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Aged 18 years and more; 2. caesarean section in parturients with placenta accreta; 3. ASA physical status classification I~II.

Exclusion criteria

Exclusion criteria: 1. Preoperative Hb 1.5 times normal value; 4. With hematological diseases; 5. Preoperative anticoagulant therapy; 6. Wiith autoimmune disease / acute fatty liver /HELLP syndrome; 7. Preoperative exist poor understanding ability, mental disorder or patients with central nervous system disorders but not cooperate.

Design outcomes

Primary

MeasureTime frame
amount of bleeding;Apgar scoring;morbidity andmortality;—

Secondary

MeasureTime frame
ICU stay;hospital stay;—

Countries

China

Contacts

Public ContactQinjun Chu

First Affiliated Hospital of Zhengzhou University

jimmynetchu@163.com+86 13643711142

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 10, 2026