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临床试验/EUCTR2008-003256-29-DE
EUCTR2008-003256-29-DE进行中(未招募)不适用

Effect of Methylnaltrexone on Postoperative Analgesic Demands

Charité – Universitätsmedizin Berlin0 个研究点开始时间: 2009年1月20日最近更新:
适应症
相关药物

试验速览

阶段
不适用
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
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Adult patients undergoing knee replacement surgery under total anaesthesia, informed consent to participate in the clinical study, capable to give written informed consent, 18-83 years
  • 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 24
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 50

排除标准

  • Chronic opioid treatment, Chronic pain with psychiatric/psychosomatic component, Abuse of drugs or alcohol, psychiatric/mental disease, Rheumatoid arthritis with chronic steroid or opioid medication, Chronic pulmonary disease with systemic steroid medication; pulmonary hypertension, Severe heart failure (NYHA>III); peripheral vascular disease, Diabetes mellitus with peripheral polyneuropathy (sensory deficit), ulcers/necrosis/infections, Paralysis, neurological deficits, Gastrointestinal dysfunction/inflammation, ileus, Acute infections, cancer, HIV, hepatitis, Pregnancy; emergency surgery, Intolerance reactions to methylnaltrexone, Participation in other trials, Surgery longer than 3 hours

研究者

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