The MyTIME clinical trial
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https://researchdata.edu.au/the-mytime-clinical-trial/2919736
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HeSANDA 1.0.0
To study is a double-blind, randomised, placebo-controlled trial of daily oral melatonin administration from 39 weeks' gestation in nulliparous pregnant women to reduce induction of labour rates. Induction of labour will be the primary endpoint of the study.
HeSANDA 1.0.0
本研究为一项双盲、随机、安慰剂对照临床试验,纳入无分娩史孕妇(nulliparous pregnant women),于妊娠39周起每日给予口服褪黑素(melatonin)以降低引产(induction of labour)率。引产发生情况将作为本研究的主要终点。



