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Clinical Trial Summary

The purpose of the study is to assess the efficacy and safety of electroacupuncture among women with pelvic organ prolapse(Level II - III), compared with sham electroacupuncture.


Clinical Trial Description

After being informed about the study and potential risk, all patients giving written informed consent form will be undergo a 1-week screening period to determine eligibility for study entry. Eligible patients will be randomly assigned to one of the two groups 1) electroacupuncture group: electroacupuncture will be provided to patients at BL33, BL35 and SP6 for 3 time per week for the first 4 weeks, then twice a week for 4 weeks, and once a week for the last 4 weeks. There will be 24 times of treatment in total in 3 month; 2) sham electroacupuncture group: sham electroacupuncture will be provided to patients at sham acupoints to BL33, BL35 and SP6 with the same schedule as electroacupuncture group.The follow-up time for the two groups are 6 months after treatment. Primary and secondary outcome will be measured at 3, 6, and 9 months from the start of the treatment, respectively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04589715
Study type Interventional
Source Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Contact Huan Chen, MsPH, MD
Phone +861088002331
Email chen.huan@live.com
Status Not yet recruiting
Phase N/A
Start date October 31, 2020
Completion date June 30, 2022

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