首页> 美国卫生研究院文献>Reproductive Medicine and Biology >Phase III trial comparing the efficacy and safety of recombinant‐ or urine‐derived human chorionic gonadotropin for ovulation triggering in Japanese women diagnosed with anovulation or oligo‐ovulation and undergoing ovulation induction with follitropin‐alfa
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Phase III trial comparing the efficacy and safety of recombinant‐ or urine‐derived human chorionic gonadotropin for ovulation triggering in Japanese women diagnosed with anovulation or oligo‐ovulation and undergoing ovulation induction with follitropin‐alfa

机译:III期临床试验比较了重组或尿液中人绒毛膜促性腺激素在诊断为无排卵或少排卵并接受卵泡促卵泡素诱导排卵的日本女性中促排卵的功效和安全性

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摘要

AimOutside of Japan, recombinant‐human chorionic gonadotropin (r‐hCG) is widely used for the induction of final follicular maturation and early luteinization in women undergoing ovulation induction; whereas in Japan, urine‐derived hCG (u‐hCG) is predominantly used. The primary objective of this study was to demonstrate the non‐inferiority of r‐hCG to u‐hCG for ovulation induction, as assessed by the ovulation rate.
机译:Aim在日本以外,重组人绒毛膜促性腺激素(r-hCG)被广泛用于诱导排卵的女性最终卵泡成熟和早期黄体化。而在日本,主要使用尿液衍生的hCG(u‐hCG)。这项研究的主要目的是证明通过排卵率评估,r-hCG相对于u-hCG的排卵诱导性不差。

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