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The improvement of surgical method for precarious placenta previa and implantation: a randomized controlled trial

The improvement of surgical method for precarious placenta previa and implantation: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023031
Enrollment
Unknown
Registered
2019-05-08
Start date
2019-05-07
Completion date
Unknown
Last updated
2019-05-13

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

Conditions

precarious placenta previa with implantation

Interventions

observation group:Bilateral internal iliac artery balloon occlusion combined with bladder predissociation of the lower uterine segment fishing-net reconstruction
control group:bladder predissociation of the lower uterine segment fishing-net reconstruction

Sponsors

Department of Obstetrics and Gynecology, the Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 18-45, with a history of cesarean section; 2. Diagnosed as precarious placenta previa, and placenta implantation was considered in preoperative ultrasound or MRI; 3. Willing to participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with heart, brain, lung, kidney, blood system and other important organ diseases; 2. Emergency surgery; 3. The patient has poor general condition and cannot tolerate the subsequent operation procedure;

Design outcomes

Primary

MeasureTime frame
Blood transfusion volume;Uterine resection rate;

Countries

China

Contacts

Public ContactChen Zhengqiong

Department of Obstetrics and Gynecology, the Second Affiliated Hospital of Army Medical University

Chenzhengqiong75@163.com+86 023-68774012

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026