Effect of Letrozole,Berberine,or Their Combination for Infertility in Women with Polycystic Ovary Syndrome:Statistical Analysis Plan for a Multicenter Randomized Controlled Trial

被引:3
作者
HongLi Ma [1 ,2 ]
JingShu Gao [2 ]
Feng Tian [3 ]
Ernest HY Ng [4 ]
XiaoKe Wu [2 ]
JianPing Liu [1 ]
机构
[1] Centre for Evidence-Based Chinese Medicine,Beijing University of Chinese Medicine
[2] Department of Obstetrics and Gynecology,First Affiliated Hospital,Heilongjiang University of Chinese Medicine
[3] Institute of Basic Research in Clinical Medicine,China Academy of Chinese Medical Sciences
[4] Department of Obstetrics and Gynaecology,The University of Hong Kong,Queen Mary Hospital
关键词
D O I
暂无
中图分类号
R711.75 [卵巢疾病];
学科分类号
100211 [妇产科学];
摘要
Introduction:Letrozole showed higher ovulation and live birth rates than clomiphene in infertile women with polycystic ovary syndrome(PCOS).Berberine,a major active component of Chinese herbal medicine rhizomacoptidis,has been used to improve insulin resistance to facilitate ovulation induction in women with PCOS,but there is no study reporting the live birth or its potential as a complementary treatment to letrozole.We aim to determine the efficacy of letrozole with or without berberine in achieving live births among 644 infertile women with PCOS in China's mainland.Methods and analysis:This is a prospective,randomized,multicentre,double-blinded,controlled design.Infertile women with PCOS were randomized into three-arm,letrozole and berberine,letrozole and berberine placebo,letrozole placebo and berberine.Data and blood were collected at baseline,the third month and sixth month after treatment,or immediately were collected if subject was pregnant.Statisticians and clinical investigators were blinded to treatment allocation and treatment related study results until the central database was locked for final data extraction and analysis determined.The statistical analysis plan described basic analysis principles,methods commonly encountered in data analysis issues,and the specific statistical procedures for analyzing the primary,secondary,and safety outcomes.Ethics and dissemination:The study was approved by the ethics committee of the First Affiliated Hospital,Heilongjiang University of Chinese Medicine.The study findings will be disseminated through peer-reviewed publications and conference presentations.Trial registration:Chinese Clinical Trial Registry:Chi CTR-TRC-09000376.Clinical Trials.gov identifier:NCT01116167.
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页码:36 / 42
页数:7
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