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Effect of Modified Traditional Chinese Medicine Hot Compress Combined with Mud Therapy on Postoperative Pain in Patients Undergoing Painless Induced Abortion

Effect of Modified Traditional Chinese Medicine Hot Compress Combined with Mud Therapy on Postoperative Pain in Patients Undergoing Painless Induced Abortion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002122
Enrollment
Unknown
Registered
2025-11-04
Start date
2025-04-02
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients undergoing painless induced abortion

Interventions

Modified hot compress pack combined with mud therapy group:Modified hot compress pack.Mud therapy
Conventional hot compress pack combined with mud therapy group:Conventional hot compress pack . Mud therapy
Control group:Conventional treatment
Mud therapy group:Mud therapy

Sponsors

Shijiazhuang Fourth Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

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

MeasureTime frame
vaginal blood loss;postoperative uterine contraction pain;duration of vaginal bleeding;

Secondary

MeasureTime frame
incidence of complications ;postoperative menstrual recovery;Quality of life score;postoperative menstrual recovery;

Countries

China

Contacts

Public ContactLiu Zhi

Shijiazhuang Fourth Hospital

277907046@qq.com13831106457

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026