EUCTR2013-000909-24-NL进行中(未招募)1 期
OPTI-CLOT:Peri-Operative PharmacokineTIc-guided dosing of CLOTting factor in Hemophilia. - OPTICLOT
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- Erasmus MC
- 入组人数
- 72
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Male
入选标准
- •- Severe and moderate hemophilia A or B (FVIII/FIX plasma level = 5%)
- •- Elective and low or medium risk surgery as defined by surgical risk score (form B)
- •- = 12 years of age at inclusion date for the randomized controlled trial;
- •- < 12 years of age at inclusion date for the PK-guided dosing observational children cohort.
- •- Written informed consent.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 72
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 42
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Patients with other congenital or acquired hemostatic abnormalities.
- •- Withdrawal of (parental) informed consent.
- •- Detectable FVIII/FIX inhibiting antibodies (>0.02 BU) at inclusion in study.
- •- General medical conditions which may interfere with participation in the study.
研究者
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