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The Treatment Outcomes of Cesarean Scar Pregnancy

The Treatment Outcomes of Cesarean Scar Pregnancy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07608094
Enrollment
82
Registered
2026-05-27
Start date
2025-08-13
Completion date
2026-12-31
Last updated
2026-06-22

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

Conditions

Cesarean Scar Pregnancy

Brief summary

A prospective randomized controlled study evaluating the impact of various treatment modalities for cesarean scar pregnancy on treatment outcomes and pregnancy outcomes

Detailed description

The excisional surgeries were conducted via excision of the cesarean scar pregnancy and closure of the uterine incision through a transvaginal approach or hysteroscopy-assisted laparoscopic approach. Conservative surgeries refer to the removal of intrauterine pregnancy tissues through ultrasound-guided vacuum aspiration or hysteroscopic surgery.

Interventions

OTHERdifferent surgical treatment

The excisional surgeries were conducted via excision of the cesarean scar pregnancy and closure of the uterine incision through a transvaginal approach or hysteroscopy-assisted laparoscopic approach. Conservative surgeries refer to the removal of intrauterine pregnancy tissues through ultrasound-guided vacuum aspiration or hysteroscopic surgery.

Sponsors

Women's Hospital School Of Medicine Zhejiang University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Women over 18 years old with a history of cesarean section 2. Ultrasound diagnosis of cesarean scar pregnancy 3. No severe internal or external diseases, such as liver disease, kidney disease, cardiovascular disease, cerebrovascular disease, etc., and able to tolerate surgery

Exclusion criteria

1. Women under the age of 18 2. CSP patients who have received treatment in other hospitals

Design outcomes

Primary

MeasureTime frameDescription
successful surgical treatmentOne day after surgerysuccessful treatment rate after surgery

Secondary

MeasureTime frameDescription
complicationOne day after surgerysevere complication rate after surgery

Countries

China

Contacts

CONTACTxiuxiu jiang, ph.D
jaingxiuxiu0418@zju.edu.cn0086-571-87061501
PRINCIPAL_INVESTIGATORxiuxiu jiang

women's hospital school of medicine Zhejiang uni

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 23, 2026