A randomized controlled clinical trial of auricular acupuncture assisted by post-installation for immediate analgesia in gynecological tumor patients with implanted acupuncture
- Conditions
- Gynecologic Oncology
- Registration Number
- ITMCTR2200005542
- Lead Sponsor
- Cancer Hospital Affiliated to University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- Not specified
1. Are aged = 18 years old 2.Female patients diagnosed with pelvic malignancies, mainly cervical cancer and endometrial cancer. 3. scheduled for brachytherapy. 4.agreement via written informed consent after being provided with an explanation regarding the purpose and characteristics of this study.
1.Serious other diseases, including liver and kidney dysfunction, acute stroke, cardiovascular diseases such as heart failure, and patients with cardiac pacemakers. 2.Regular use of painkillers or use of other pain relieving medicine on the day of the brachytherapy. 3. Known hypersensitive reaction to acupuncture treatment or the inability to cooperate with the acupuncture procedure. 4.Abnormal skin conditions in specific areas that may prevent acupuncture treatment. 5.Having a tendency to bleed easily. 6.Patients with history of syncope or seizure. 7. Patients who do not agree to clinical trials or those who have participated in other clinical trials in hospital. 8.Other people deemed unsuitable for participation by the researcher and atients incapable of reading, understanding, and signing a written consent form (for example,people who are mentally retarded, blinded,illiterate, or foreigners).
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS;
- Secondary Outcome Measures
Name Time Method SAS;Nausea and vomiting;Bruggemann comfort scale (BCS);SDS;