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临床试验/CTIS2024-515579-36-00
CTIS2024-515579-36-00
进行中(未招募)
1 期

Hydroxychloroquine treatment for Recurrent Pregnancy Loss: a randomized double-blind placebo-controlled trial

Hvidovre Hospital0 个研究点目标入组 186 人2024年7月3日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Recurrent Pregnancy Loss
发起方
Hvidovre Hospital
入组人数
186
状态
进行中(未招募)
最后更新
去年

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2024年7月3日
结束日期
待定
最后更新
去年
研究类型
Interventional clinical trial of medicinal product

研究者

入排标准

入选标准

  • \= 4 confirmed consecutive pregnancy losses prior to gestational age 22\+0 in women with unexplained recurrent pregnancy loss (RPL), \= 3 confirmed consecutive pregnancy losses prior to gestational age 22\+0 in women with unexplained RPL with minimum one second trimester loss

排除标准

  • Age \< 18 years or \> 40 years, Previous HCQ treatment in relation to conceive, \> 1 previous live birth., Previous participation in current study., Prominent uterine abnormalities detected by hysterosalpingography/hysteroscopy or hydrosonography, Known prominent chromosome abnormalities for the couple trying to conceive, A menstrual cycle \< 23 days or \> 35 days if the pregnancy is conceived naturally. If the woman received fertility treatment the menstrual cycle has no consequence., Detection of positive lupus\-anticoagulant or positive IgG/IgM for anticardiolipin\-antibodies (\=10 GPL kU/l, measured at the same laboratories at the Capital Region of Denmark) or plasma homocysteine \=25 microgram/l by repeated measurements 12 weeks apart before the pregnancy., Positive HIV test or test indicating chronic hepatitis B or C., Psoriasis, retinopathic or serious hearing deficiency (contraindication for treatment with HCQ), Current chronic disease implicating a constant consumption of immunomodulatory medicine or medicine potentially harmful to the pregnancy/embryo, Hgb \= 6\.5 mmol/L, leucocytes \< 3\.5 E9/L, thrombocytes \< 145 E9/L by the time of inclusion

结局指标

主要结局

未指定

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