Patients undergoing painless induced abortion
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Diagnosed with intrauterine early pregnancy; 2) Aged between 20 and 40 years; 3) Voluntarily agree to undergo painless induced abortion for pregnancy termination; 4) Normal intraoperative monitoring indicators (heart rate, blood pressure, respiration, oxygen saturation, and pulse) under propofol injection anesthesia; 5) Pain assessment score of 1–6 points using the Numerical Rating Scale (NRS).
Exclusion criteria
Exclusion criteria: Menopause for over 1 year; 2) Pregnancy termination within the past 6 months, history of induced abortion =2 times within 1 year, or total induced abortion history =3 times; 3) Within 6 months post-cesarean section, within 3 months post-full-term delivery, or during lactation; 4) Prolonged use of steroidal contraceptives; 5) Reproductive system tumors, genital malformations; 6) Highly anteverted/retroverted uterus, difficult cervical exposure, or spinal/pelvic disorders causing difficulty in lithotomy positioning; 7) History of placenta accreta or postpartum hemorrhage; 8) Skin lesions/edema/dermatological conditions at acupoint sites, allergy to study medications, or adhesive tape allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| vaginal blood loss;postoperative uterine contraction pain;duration of vaginal bleeding; | — |
Secondary
| Measure | Time frame |
|---|---|
| incidence of complications ;postoperative menstrual recovery;Quality of life score;postoperative menstrual recovery; | — |
Countries
China
Contacts
Shijiazhuang Fourth Hospital