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The bleeding scoring system for cesarean scar pregnancy: a randomized controlled trial

The bleeding scoring system for cesarean scar pregnancy: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008584
Enrollment
Unknown
Registered
2016-06-02
Start date
2016-07-01
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

cesaran scar pregnancy

Interventions

experimental group:Use the risk scoring system for CSP to guide treatment

Sponsors

West China Second University Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. All patients with previous cesarean delivery were lower uterine segment crosscutting cesarean delivery; 2. Patients were diagnosed based on serum ß-hCG and ultrasonography, and ultrasonographic diagnosis was made using the following criteria: (1) an empty uterine cavity with a clearly demonstrated endometrium; (2) an empty cervical canal; (3) a gestational sac, with or without fetal cardiac activity, located in the anterior portion of the lower uterine segment at the presumed site of the caesarean scar; and (4) a thinned or absent myometrium between the gestational sac and the bladder (less than 0.5 cm); 3. Dilatation and suction evacuation were the main treatment for patients.

Exclusion criteria

Exclusion criteria: 1. Prior to hospital, patients had recieved treatment such as drug miscarriage or abortion; 2. Patients who recieved surgical resection or conservative treatment as main treatment; 3. Patients who were unable to undergo an operation due to other complications.

Design outcomes

Primary

MeasureTime frame
intra-operative blood loss;percentage of excessive blood loss;

Secondary

MeasureTime frame
hospitalization days;blood ß-hCG dropped to normal time;recovery period of time;

Countries

China

Contacts

Public ContactBian Ce

West China Second University Hospital, Sichuan University

zhaoxia21212@163.com+86 15884580956

Outcome results

None listed

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