ACTRN12606000269538尚未招募3 期
A prospective, dose ranging effectiveness study of sustained-release opioids in the subjective sensation of dyspnoea in opioid naive patients in the palliative care setting.
Repatriation General Hospital0 个研究点目标入组 100 人开始时间: 2006年6月29日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 ot stated（—）
- 性别
- All
入选标准
- •Specialist relevant has assessed participant to have received maximal treatment (including reversing anaemia) • On stable medications for the previous 7 days• Participant has dyspnoea score greater than or equal to 2 on the Modified Medical Research Council dyspnoea scale • In the treating clinician's estimation, the participant has a prognosis of at least one month.• On stable oxygen needs.
排除标准
- •Pregnancy, any chance of pregnancy, or breastfeeding• On regular opioid medications, including codeine preparations. • Confusion (MMSE<24/30)• AKPS score of <50• Uncontrolled nausea or vomiting.• True adverse reaction(s) or hypersensitivity to previous opioids.• A creatinine clearance of <15ml/min. • Gastrointestinal obstruction.• Concomitant use of Monoamine Oxidase Inhibitor(s) (MAOIs) in the last 2 weeks.• Past history of substance misuse• Unwilling or unable to complete study measures.
研究者
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