Comparison of clinical effects of abdominal aortic balloon occlusion and uterine artery embolization in the treatment of cesarean section scar pregnancy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900023683

Enrollment

Unknown

Registered

2019-06-07

Start date

2019-09-01

Completion date

Unknown

Last updated

2019-06-11

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

Conditions

Cesarean section scar pregnancy

Interventions

experimental group: Shù qián anzhì fù zhu dòngmài qiú náng 10/5000 Preoperative placement of abdominal aortic balloon

Control group:Preoperative bilateral uterine artery embolization

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. pregnant women aged 18-35 years; 2. less than 12 weeks of gestational age; 3. imaging diagnosis of cesarean section scar pregnancy type II or III.

Exclusion criteria

Exclusion criteria: 1. coagulation abnormalities; 2. thrombosis; 3. abdominal aortic dissection or deformity; 4. renal function insufficiency; 5. Chronic hypertension.

Design outcomes

Primary

Measure	Time frame
Amount of bleeding;operation time;Hospital stay;Radiation dose;Hormone level;Menstrual volume;	—

Countries

China

Contacts

Public ContactZhao Hu

Chengdu Women and Children's Central Hospital

zhaoh1976@163.com+86 13881969153

Outcome results

None listed

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