EUCTR2006-002208-32-GB进行中（未招募）不适用
A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting - Oral versus IV paracetamol
York Hospital NHS Trust0 个研究点开始时间: 2006年9月18日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •All patients on the list for day case knee arthroscopy aged between 18 to 60 years and weighing between 50 to 90 kg will be eligible for the 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
- •Age <18 and >60 years, ASA 3 or 4 (American society of anaestesiologist classification - ASA 3 & 4 are sicker patients than ASA 1 & 2), known allergy to paracetamol, patients who had paracetamol in the last 12 hours, pregnant or breast feeding women, history of complete non-responsiveness to acetaminophen, inflammatory bowel disease, chronic pain patients, arthroscopies related to infection (where surgeon would not instil local anaesthetic), bilateral arthroscopies.
研究者
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