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临床试验/EUCTR2012-005063-28-SE
EUCTR2012-005063-28-SE进行中(未招募)1 期

Release of substance P during peritoneal dialysis: effects of intervention. Controlled cross-over study of the neurokinin-1 receptor antagonist Aprepitant

niversity of Gothenburg0 个研究点目标入组 32 人开始时间: 2012年11月9日最近更新:
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
入组人数
32

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
All

入选标准

  • Included persons are treated with PD since at least 3 months and are males aged 20-90 or post-menopausal females up to age 90.
  • Included persons must have positive ultrafiltration (ultrafiltration volume larger than 0 ml/24 hours measured not more than one month earlier).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 16
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 16

排除标准

  • Moderate to serious liver damage, potential or known damage to the blood-brain barrier (e.g. brain tumor, meningitis, encephalitis), peritonitis during the last two months and treatment with any of the following drugs: warfarin, corticosteroider, pimozid, terfenadin, astemizol, cisaprid, ciklosporin, takrolimus, sirolimus, everolimus, alfentanil, diergotamin, ergotamin, fentanyl, kinidin, rifampicin, fenytoin, karbamazepin, fenobarbital och metotrexat.

研究者

发起方
niversity of Gothenburg

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