Postoperative Analgesia for Induced Abortion
Conditions
Interventions
treatment group:low intensity focused ultrasound therapy
Sponsors
Sichuan Provincial Maternity and Child Health Care Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Age >= 18 years; 2. Patients with early intrauterine pregnancy undergoing induced abortion for pregnancy termination; 3. Patients with a post-abortion NRS (Numerical Rating Scale) pain score >= 4; 4. Signed informed consent and voluntary participation in the trial.
Exclusion criteria
Exclusion criteria: 1. Patients with skin lesions at the intended treatment site, such as ulceration, infection, or large blisters; 2. Individuals with cognitive impairment who are unable to communicate or cooperate; 3. Patients with metallic implants in the uterine cavity; 4. Patients who experienced major complications during the abortion procedure, such as severe hemorrhage or uterine perforation; 5. Patients who have participated in other clinical trials within the past three months; 6. Any other conditions deemed by the investigator as unsuitable for trial participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NRS (Numerical Rating Scale) pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| 15-minute post-treatment NRS score reduction value;patient departure time;NRS score reduction at departure; | — |
Countries
China
Contacts
Public ContactLi Shengmei
Sichuan Provincial Maternity and Child Health Care Hospital
Outcome results
None listed