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临床试验/NCT00296465
NCT00296465已完成2 期

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Three Dosage Strengths of Pulsatile GnRH Administered Intravenously or Subcutaneously (Via Portable Infusion Pump) Compared to Oral Treatment With Clomiphene Citrate in Anovulatory or Oligoovulatory Infertile Females

Ferring Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2005年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
132
试验地点
1
主要终点
Pregnancy rate

研究概览

简要总结

This study will be performed in approximately 132 women with anovulatory/oligoovulatory infertility.

详细描述

This multicenter, randomized, double-blind, placebo-controlled study will be performed in approximately 132 women with anovulatory/oligoovulatory infertility. The treatment duration will be approximately 4 weeks with pulsatile GnRH or placebo and 5 days with Clomiphene Citrate or placebo. All subjects will be screened based on inclusion/exclusion criteria, medical/infertility history and general safety assessments. Subjects that complete screening will be dispensed 100 mg of oral progesterone twice a day for 10 days to induce uterine bleeding. On Cycle Day 5 from the start of bleeding the subject will be randomly assigned to 1 of 7 treatment groups. All subjects will be monitored weekly throughout the 4 week treatment period for ovulation and intercourse will be timed. All subjects will be required to return to the study center for a total of 8 visits. In addition, all subjects with a confirmed clinical pregnancy will be monitored until fetal heartbeat is confirmed at approximately 5-6 weeks gestation

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Placebo IV

Placebo Comparator

Placebo Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Pulsatile GnRH (Drug)

Lutrepulse® 5mcg IV

Experimental

5.0 mcg Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Pulsatile gonadotropin-releasing hormone (GnRH) (Drug)

Lutrepulse® 5mcg IV

Experimental

5.0 mcg Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Clomiphene Citrate (Drug)

Lutrepulse® 10 mcg IV

Experimental

10.0 mcg Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Pulsatile gonadotropin-releasing hormone (GnRH) (Drug)

Lutrepulse® 10 mcg IV

Experimental

10.0 mcg Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Clomiphene Citrate (Drug)

Lutrepulse® 20 mcg SC

Experimental

20.0 mcg Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Pulsatile gonadotropin-releasing hormone (GnRH) (Drug)

Lutrepulse® 20 mcg SC

Experimental

20.0 mcg Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Clomiphene Citrate (Drug)

Placebo IV

Placebo Comparator

Placebo Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Clomiphene Citrate (Drug)

Placebo SC

Placebo Comparator

Placebo Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Pulsatile GnRH (Drug)

Placebo SC

Placebo Comparator

Placebo Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks and oral placebo clomiphene citrate for 5 days

干预措施: Placebo Clomiphene Citrate (Drug)

Clomiphene Citrate/Placebo IV

Active Comparator

Oral clomiphene citrate (over encapsulated) for 5 days and Placebo Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks

干预措施: Clomiphene Citrate (Drug)

Clomiphene Citrate/Placebo IV

Active Comparator

Oral clomiphene citrate (over encapsulated) for 5 days and Placebo Pulsatile GnRH (Lutrepulse®) administered intravenously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks

干预措施: Placebo Pulsatile GnRH (Drug)

Clomiphene Citrate / Placebo SC

Active Comparator

Oral clomiphene citrate (over encapsulated) for 5 days and Placebo Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks

干预措施: Clomiphene Citrate (Drug)

Clomiphene Citrate / Placebo SC

Active Comparator

Oral clomiphene citrate (over encapsulated) for 5 days and Placebo Pulsatile GnRH (Lutrepulse®) administered subcutaneously via portable infusion pump in a pulsatile fashion (every 90 minutes) for 4 weeks

干预措施: Placebo Pulsatile GnRH (Drug)

结局指标

主要结局

Pregnancy rate

时间窗: Day 16

次要结局

  • Adverse events, including ovarian hyperstimulation syndrome (OHSS)(Day 1 to week 5)

研究者

申办方类型
Industry

研究点 (1)

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