Endometrial injury
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Females aged 15 to 49 years; 2. Meet the indications for induced abortion as stipulated in the "Clinical Diagnosis and Treatment Guidelines and Technical Operation Specifications: Family Planning Volume"; 3. Diagnosis of intrauterine pregnancy confirmed by color Doppler ultrasound and serum hCG testing; 4.Voluntary participation in this study with provision of informed consent.
Exclusion criteria
Exclusion criteria: 1. Presence of any contraindication to induced abortion; 2. Local skin lesions such as ulcerations, infections, or bullous dermatological conditions at the treatment site; 3. Uncontrolled systemic diseases (e.g., Disseminated Intravascular Coagulation); 4. Voluntary withdrawal from the study or poor compliance (failure to complete the scheduled three LIFU treatment sessions).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Uterine Size;Endometrial Thickness; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence and type of all adverse events;Total amount of vaginal bleeding, duration of vaginal bleeding, time to menstrual resumption, and complication rate.;Inflammatory markers: White blood cell count, lymphocyte percentage, neutrophil percentage, and C-reactive protein.;Pain; | — |
Countries
China
Contacts
The international peace maternity and child health hospital