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A randomized controlled clinical trial for the effect of FUAS combined with suction curettage and simple suction curettage in the treatment of type II cesarean scar pregnancy

A randomized controlled clinical trial for the effect of FUAS combined with suction curettage and simple suction curettage in the treatment of type II cesarean scar pregnancy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034332
Enrollment
Unknown
Registered
2020-07-02
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

cesarean scar pregnancy

Interventions

experimental group:FUAS combined with suction curettage
control group:pure suction curettage

Sponsors

Qingdao Women and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. History of cesarean section in lower uterine segment; 2. Menopause history (within 8 weeks) and serum ß - hCG positive; 3. CSP type II (Chinese Medical Association classification standard), gestational sac diameter less than 5.0 cm; 4. Voluntary choice of FUAS and / or hysteroscopy.

Exclusion criteria

Exclusion criteria: 1. Vaginitis or vaginal bleeding greater than menstrual volume 2. Severe coagulation dysfunction,Severe internal and external diseases,Contraindication of anesthesia 3. Positioning losers 4. Allergy to sulfur hexafluoride or related drugs or Lactation.

Design outcomes

Primary

MeasureTime frame
intraoperative hemorrhage;—

Secondary

MeasureTime frame
cure rate;—

Countries

China

Contacts

Public ContactShuping Zhao

Qingdao Women and Children's Hospital

zhaosp66@126.com+86 13325027766

Outcome results

None listed

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