ISRCTN28898435
已完成
不适用
Does fluid administration in the terminally ill reduce the frequency and amount of sedation required for the management of agitation/restlessness?
HS R&D Regional Programme Register - Department of Health (UK)0 个研究点目标入组 0 人2004年1月23日
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- Symptoms and general pathology
- 发起方
- HS R&D Regional Programme Register - Department of Health (UK)
- 状态
- 已完成
- 最后更新
- 11年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Patients who meet the inclusion criteria will be identified during the daily team meetings held within each of the hospices. The inclusion criteria are as follows:
- •1\. Deemed to have a short life expectancy (Bozetti 1996\)
- •2\. Aged above 18
- •3\. Inpatient within Butterick Hospice, Teesside Hospice, Hartlepool Hospice, St Oswalds Hospice or the Newcastle Marie Curie Centre
- •4\. Oral intake has fallen below 1000 ml/24 hour and is recognised by the team as part of their deterioration
排除标准
- •1\. Known to have cerebral oedema
- •2\. Known to have congestive cardiac failure
- •3\. Known to have a coagulation disorder
- •4\. Known to be in renal or liver failure or are hypercalcaemic
- •5\. Known to have a tumour which has a direct influence on fluid balance
结局指标
主要结局
未指定
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