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临床试验/NCT01266421
NCT01266421已完成不适用

International Active Surveillance Study of Medication Used for the Treatment of Endometriosis: Visanne Post-approval Observational Study

Center for Epidemiology and Health Research, Germany1 个研究点 分布在 1 个国家目标入组 27,840 人开始时间: 2010年12月7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
入组人数
27,840
试验地点
1
主要终点
Anemia

研究概览

简要总结

The study assesses safety aspects of Dienogest (DNG) 2mg/day (Visanne) used as endometriosis therapy and of other hormonal treatments for endometriosis.

详细描述

Endometriosis is a common, chronic, gynecological disease characterized by pain and impaired fertility. It causes chronic inflammation, ovarian cyst formation, fibrosis and adhesions. Symptoms seem to respond to decreased circulating estrogen. The mainstay of medical treatment is hormonal induced anovulation and a reduction in endogenous estrogen production.

Medications for endometriosis such as Danazol and GnRH agonists have clinically relevant side-effects limiting treatment duration with these medications to 6-12 months.

Dienogest (DNG) is a 19-nortestosterone derivative progestogen. DNG 2mg/day is a reliable and effective treatment for dysmenorrhea, premenstrual pain, dyspareunia and diffuse pelvic pain associated with endometriosis.

Two important class effects of progestogens are the induction of bleeding disturbances and their influence on mood disturbance. It is not known what influence DNG will have on bleeding disturbances associated with endometriosis, particularly over a longer time frame.

In addition, women who suffer from endometriosis are at high risk of developing depressive symptoms. It is difficult to differentiate if depressive symptoms are causally associated with progestogen use or sequela of the disease process.

研究设计

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

入排标准

性别
Female
接受健康志愿者

入选标准

  • Women using a newly prescribed regimen for endometriosis (first-time users or switchers or re-starters)
  • Women who are willing to participate in this long-term follow-up study

排除标准

  • Women who are not cooperative/available for follow-up
  • Women with a language barrier

结局指标

主要结局

Anemia

时间窗: Within 6 years

Medical intervention for anemia induced by cyclical bleeding disturbances (anemia)

Depression

时间窗: Within 6 years

First time occurence of clinically relevant depression, or worsening of existing depression

次要结局

未报告次要终点

研究者

发起方
Center for Epidemiology and Health Research, Germany
申办方类型
Other
责任方
Principal Investigator
主要研究者

Klaas Heinemann, MD, PhD

Principal Investigator

Center for Epidemiology and Health Research, Germany

研究点 (1)

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