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A multicenter randomized trial of personalized acupuncture, fixed acupuncture, letrozole, and placebo letrozole on live birth in infertile women with polycystic ovary syndrome

Authors :
Shiya Huang
Min Hu
Ernest Hung Yu Ng
Elisabet Stener-Victorin
Yanhua Zheng
Qidan Wen
Cong Wang
Maohua Lai
Juan Li
Xingcheng Gao
Xinhua Wang
Zhenxing Hu
Tian Xia
Rongkui Hu
Jianping Liu
Xiaohui Wen
Shuna Li
Kewei Quan
Xingyan Liang
Hongcai Shang
Hongxia Ma
Jie Qiao
Source :
Trials, Vol 21, Iss 1, Pp 1-16 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Background Traditional Chinese medicine (TCM) usually involves syndrome differentiation and treatment. Acupuncture, one form of TCM, requires the selection of appropriate acupoints and needling techniques, but many clinical trials on acupuncture have used fixed acupuncture protocols without accounting for individual patient differences. We have designed a multicenter randomized controlled trial (RCT) to evaluate whether personalized or fixed acupuncture increases the likelihood of live births in infertile women with polycystic ovary syndrome (PCOS) compared with letrozole or placebo letrozole. We hypothesize that letrozole is more effective than personalized acupuncture, which in turn is more effective than fixed acupuncture, and that placebo letrozole is the least effective intervention. Moreover, we hypothesize that personalized acupuncture is more likely to reduce the miscarriage rate and the risk of pregnancy complications compared with letrozole. Methods/design The study is designed as an assessor-blinded RCT. A total of 1100 infertile women with PCOS will be recruited from 28 hospitals and randomly allocated to 4 groups: personalized acupuncture, fixed acupuncture, letrozole, or placebo letrozole. They will receive treatment for 16 weeks, and the primary outcome is live birth. Secondary outcomes include ovulation rate, conception rate, pregnancy rate, pregnancy loss rate, changes in hormonal and metabolic parameters, and changes in quality of life scores. Adverse events will be recorded throughout the trial. All statistical analyses will be performed using IBM SPSS Statistics version 21.0 software (IBM Corp., Armonk, NY, USA), and a P value

Details

Language :
English
ISSN :
17456215
Volume :
21
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.42813bae1f8548dc9411438a03be43c3
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-020-4154-1