CTRI/2022/04/041870进行中(未招募)4 期
Phase IV study to assess the safety and effectiveness ofDienogest (Visanne®) amongst Indian women withEndometriosis, in real-world clinical practice: the VISAGEStudy - VISAGE
试验速览
- 阶段
- 4 期
- 状态
- 进行中(未招募)
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Female patients in India at least 18 years of age
- •Clinical or surgical diagnosis of endometriosis: Clinical diagnosis by suggestive symptoms
- •and positive finding in imaging study (Chocolate cyst)
- •Patients diagnosed with endometriosis associated pelvic pain who have not been previously
- •treated with Dienogest
- •Decision to initiate treatment with Dienogest was made as per investigator’s routine
- •treatment practice
- •Signed informed consent
排除标准
- •Participation in an investigational program with interventions outside of routine clinical
- •Contra-indications according to the local summary of product characteristics (SPC)
研究者
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