跳至主要内容
临床试验/EUCTR2005-002369-35-DE
EUCTR2005-002369-35-DE进行中(未招募)1 期

Reduction of pain under pressure of an experimentally induced hematoma in healthy volunteers by two Bromelain preparations (Bromelain-POS(R) and Traumanase(R) forte). - Bromelain-Häma-2P

rsapharm Arzneimittel GmbH&Co. KG0 个研究点目标入组 140 人开始时间: 2006年5月11日最近更新:
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
140

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

  • - healthy subject of either sex
  • - aged between 18 and 40 years
  • - written informed consent signed
  • - willing to fulfill the study requirements regarding measures taken, number of visits, questions asked and duration of study
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - regular concomitant treatment with anti-inflammatory or analgesic drugs
  • - known intolerability of the test drugs or inactive ingredients thereof
  • - known intolerability of pineapples
  • - hemorrhagic diathesis
  • - continuing concomitant medication for less than 2 months
  • - participation in a clinical study less than 30 days prior to study onset
  • - simultaneous participation in another clinical study
  • - women of childbearing potential without sufficient contraception
  • - women refusing a pregnancy test (HCG-method) at the onset of the study
  • - pregnancy or nursing mother
  • - values of <0.2 kp/cm² or >5.0 kp/cm² on the scale of the pressure gauge during the screening measurements
  • - difference of >0.2 kp/cm² in the right-left comparison during the screening measurements

研究者

发起方
rsapharm Arzneimittel GmbH&Co. KG

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