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A randomized clinical trial comparing the efficacy of drug and artificial abortion.

Comparion of the treatment efficacy for between combination drug mifepristone and misoprostol abortion and B ultrasound-guided curettage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007664
Enrollment
Unknown
Registered
2015-12-28
Start date
2016-01-01
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

arrested pregnancy with 14 week's gestation

Interventions

one:mifepristone and misoprostol
two:Curettage

Sponsors

Reproductive Hospital Affiliated to Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 39 Years

Inclusion criteria

Inclusion criteria: 1. be diagnosed as embryo stop by double B ultrasound diagnosis after pregnancy; 2. Gestational weeks 5-13; 3. Gestational sac size less than 5cm; 4. Younger than 40 years old; 5. No previous uterine surgery (excluding hysteroscopy).

Exclusion criteria

Exclusion criteria: 1. Suffering from adrenal disease, diabetes and other endocrine disorders, liver and kidney with dysfunction. 2. Suffering from abnormal blood disease 3. Anemia (hemoglobin 130 mmHg and (or) diastolic blood pressure>90mmHg, 1mmHg = 0.133kPa), hypoglycemia (SBP = 2 degrees, have not yet reached normal (<= 1 degree); 6. Placenta previa with abnormal position; 7. IUD merger pregnancy; 8. Ectopic pregnancy including special parts: uterine scar parts pregnancy, cervical pregnancy, uterine horn pregnancy and so on; 9. Allergies, there is a serious history of drug allergy; 10. Smoking more than 15/d or alcohol addicts.

Design outcomes

Primary

MeasureTime frame
endometrial thickness;

Secondary

MeasureTime frame
live birth rate;menstrual bleeding;miscarriage rate;

Countries

China

Contacts

Public ContactYan Lei
yanleiandu@163.com+86 18660782393

Outcome results

None listed

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