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临床试验/NCT01075854
NCT01075854已完成不适用

A Prospective, Multi-center, Observational Study of Gonal-F Filled by Mass Pens in Multifollicular Stimulation Prior to IVF/ICSI

Merck KGaA, Darmstadt, Germany1 个研究点 分布在 1 个国家目标入组 1,539 人开始时间: 2009年4月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
1,539
试验地点
1
主要终点
Efficacy

研究概览

简要总结

This is a prospective, observational study in women using Gonal-F filled-by-mass (FbM) in ovarian hyperstimulation as part of their in-vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) treatment at infertility clinics in Korea. The purpose of this study is to assess Gonal-F FbM in a practical setting encompassing all subject groups and local practices.

详细描述

Follicle stimulating hormone (FSH) is a complex hetero-dimeric glycoprotein used therapeutically to stimulate follicular development in the ovary. The technical advance of recombinant technology to manufacture FSH has resulted in a biochemically pure FSH preparation with high batch-to-batch consistency. The protein content can be reliably quantified in mass units by size exclusion high performance liquid chromatography. These developments have enabled recombinant human FSH follitropin alfa (Gonal-F) to be filled and released in vials on the basis of mass with a variability of only ±2%. In one study, the FbM batches appeared to deliver a more consistent therapeutic effect than the filled-by-bioassay batches. In another randomized trial, self-administration and subjects' satisfaction were significantly higher in the pen device group than the conventional syringe group. Local reactions at injection sites and pain were significantly higher in the conventional syringe group than in the pen device group. The authors concluded that the pen device of Gonal-F is safe, convenient, and less painful, with more subject satisfaction than the conventional syringe form.

This prospective, multicentric, observational study is planned in women using Gonal-F FbM in ovarian hyperstimulation as part of their IVF/ICSI treatment at infertility clinics in Korea. Subjects fulfilling the eligibility criteria shall be enrolled in a consecutive manner over a 9-month period (approximately 1500 subjects).

OBJECTIVES

Primary objective:

  • To assess the effectiveness Gonal-F FbM

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Women who are prescribed Gonal-F FbM by their treating physician for their IVF/ICSI treatment cycle will be eligible for this study

排除标准

  • Subjects who have hypersensitivity to follitropin alfa, FSH or to any of the excipients
  • Subjects with tumors of the hypothalamus and pituitary gland
  • Ovarian enlargement or cyst not due to polycystic ovarian disease
  • Gynecological hemorrhages of unknown etiology
  • Ovarian, uterine or mammary carcinoma
  • Primary ovarian failure
  • Malformations of sexual organs incompatible with pregnancy
  • Fibroid tumors of the uterus incompatible with pregnancy

结局指标

主要结局

Efficacy

时间窗: Start of treatment to confirmation of pregnancy

Number of oocytes retrieved and clinical pregnancy rate per cycle

次要结局

  • Efficacy, Safety and Convenience(Start of treatment to confirmation of pregnancy)

研究者

申办方类型
Industry

研究点 (1)

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