Early induced abortion
Conditions
Interventions
study group:Administer 25 µ g misoprostol vaginal tablets 1.5 hours before surgery
control group:Take 400 µ g misoprostol tablets orally 2.5 hours and 0.5 hours before surgery, respectively
Sponsors
Women’s Hospital, Zhejiang University School of Medicine
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. 18 years old< = age< = 40 years old; 2. Confirmed intrauterine pregnancy, gestational age of 10-12 weeks, meeting the indications for abortion surgery; 3. No contraindications to abortion, planned to undergo forceps curettage to terminate pregnancy; 4. Voluntarily sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Allergic to prostaglandin drugs; 2.History of cervical surgery (such as cervical conization, cervical electrocautery, cervical laser, etc.); 3.Existence of cervical diseases (such as cervical incompetence, cervical fibroids, cervicitis, cervical precancerous lesions, etc.); 4.Have taken or received medications or treatments that may affect cervical dilation; 5.Accompanied by abnormal mental state or cognitive impairment, unable to cooperate with research; 6.Other situations deemed unsuitable for inclusion by researchers;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effective rate of cervical dilation (8.5mm pass rate); | — |
Secondary
| Measure | Time frame |
|---|---|
| Cervical dilation diameter (the maximum diameter that the cervical dilation rod can pass through before surgery); Surgical operation time (from the insertion of the intrauterine probe to the end of su; | — |
Countries
China
Contacts
Public ContactJiang Xiuxiu
Women’s Hospital, Zhejiang University School of Medicine
Outcome results
None listed