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Clinical Trials/ITMCTR2200005542
ITMCTR2200005542
Not yet recruiting
Phase 1

A randomized controlled clinical trial of auricular acupuncture assisted by post-installation for immediate analgesia in gynecological tumor patients with implanted acupuncture

Cancer Hospital Affiliated to University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Gynecologic Oncology
Sponsor
Cancer Hospital Affiliated to University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Sponsor
Cancer Hospital Affiliated to University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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).

Outcomes

Primary Outcomes

Not specified

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