artificial abortion
Conditions
Interventions
Test group:Low-intensity focused ultrasound+postoperative anti-infection and hemostasis treatment
control group:Anti-infection and hemostasis treatment after operation
Sponsors
Tianjin Medical University General Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1) Female aged 18-40; 2) Previous menstrual pattern; 3) Pregnancy time 6-10 weeks; 4) Ultrasound indicates intrauterine pregnancy; 5) No contraindication of induced abortion; 6) Subjects voluntarily and signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1) Patients with benign and malignant tumors and other systemic diseases in the pelvis and abdomen; 2) There are skin problems such as ulceration, infection and blisters on the skin of the treatment site; 3) Clinical diagnosis of missed abortion; 4) Patients with uterine leiomyoma, adenomyosis and uterine malformation; 5) Those suffering from serious mental illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endometrial thickness; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative uterine contraction pain;Postoperative vaginal bleeding time;Postoperative vaginal bleeding;Menstrual rehydration time;Uterine artery blood perfusion index;Postoperative uterine size;Postoperative complications; | — |
Countries
China
Contacts
Public ContactGuXiangYing
General Hospital of Tianjin Medical University
Outcome results
None listed