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临床试验/NCT03586063
NCT03586063已完成不适用

A Multicenter Observational Study of Diphereline 3.75 mg Treatment Effectiveness in Russian Women Suffering From Internal Genital Endometriosis

Ipsen34 个研究点 分布在 1 个国家目标入组 465 人开始时间: 2011年11月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Ipsen
入组人数
465
试验地点
34
主要终点
Severity of disease symptom menorrhagia (none-mild-moderate-severe) in different disease stages I, II, III in the Russian subject population scheduled for treatment with Diphereline 3.75 mg

研究概览

简要总结

To describe Gonadotropin-Releasing Hormone agonists (GnRH-a) treatment effectiveness on reduction of internal genital endometriosis symptom - menorrhagia - in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3,75 mg - assessment performed six months after the last injection.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Premenopausal women aged 25-40 years old
  • With symptomatic internal genital endometriosis - at least mild menorrhagia present or worse
  • Internal genital endometriosis diagnosis is based on enlarged uterus detected by pelvic bimanual examination and ultrasound examination (stages I-II-III by Demidov in accordance with ultrasound results not earlier than 2 months before first injection
  • Naive patients who have never been prescribed a GnRH agonist

排除标准

  • Pregnant subjects
  • Subjects with hypersensitivity to GnRH analogue or to one of its excipients
  • Subjects treated with any other investigational drug within the last 30 days before study entry
  • Subjects' refusal to participate in the study

结局指标

主要结局

Severity of disease symptom menorrhagia (none-mild-moderate-severe) in different disease stages I, II, III in the Russian subject population scheduled for treatment with Diphereline 3.75 mg

时间窗: Change from baseline to up to 6 months after the last injection (up to month 11)

A responder is defined as a subject with menorrhagia reduction at least by one level (i.e. from severe to moderate, from moderate to mild, from mild to none).

次要结局

  • Patients' age at study entry(Baseline (Day 1))
  • Gynaecological history(Baseline (Day 1))
  • Internal genital endometriosis symptom dysmenorrhea in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(Change from baseline (Day 1) to 6 months after the last injection (up to Month 11))
  • Reproduction function will be assessed by the number of patients who avoided hysterectomy/ did not receive a surgical treatment 6 and 9 months after the end of treatment with Diphereline 3.75mg(6 and 9 months after the end of treatment with Diphereline)
  • Age at the time of internal genital endometriosis diagnosis(Baseline (Day 1))
  • Concomitant medications and non drug therapy for internal endometriosis treatment(Baseline (Day 1))
  • Severity of disease symptom dysmenorrhea (none-mild-moderate-severe) in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(On the day of the last injection (up to Month 5))
  • Reproduction function will be assessed by the number of patients got pregnant 6 and 9 months after the end of treatment with Diphereline 3.75mg(6 and 9 months after the end of treatment with Diphereline)
  • Medical history(Baseline (Day 1))
  • Severity of disease symptom menorrhagia (none-mild-moderate-severe) in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(On the day of the last injection (up to Month 5))
  • Uterine volume in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(Baseline (Day 1) and on the day of the last injection (up to Month 5))
  • Internal genital endometriosis symptom metrorrhagia in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(Change from baseline (Day 1) to 6 months after the last injection (up to Month 11))
  • Internal genital endometriosis symptom pelvic pain in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(Change from baseline (Day 1) to 6 months after the last injection (up to Month 11))
  • Diphereline 3.75 mg treatment practice will be assessed by patient compliance with treatment schedule (each 28 days) in line with treatment administration approved in Russian Federation(Up to Month 5)
  • Data on fertility: primary and secondary sterility(Baseline (Day 1))
  • Uterine shape (bimanual pelvic examination) in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(Baseline (Day 1) and on the day of the last injection (up to Month 5))
  • Severity of disease symptom metrorrhagia (none-mild-moderate-severe)(On the day of the last injection (up to Month 5))
  • Severity of disease symptom pelvic pain (none-mild-moderate-severe) in different disease stages I, II, III in the Russian patient population scheduled for treatment with Diphereline 3.75 mg(On the day of the last injection (up to Month 5))
  • Diphereline 3.75 mg treatment practice will be assessed by the number of scheduled/ performed injections with treatment schedule (each 28 days) in line with treatment administration approved in Russian Federation(Up to Month 5)

研究者

发起方
Ipsen
申办方类型
Industry
责任方
Sponsor

研究点 (34)

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