NL-OMON54708招募中不适用
*The iLIVE medication optimisation trial* - iLIVE medication study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 110
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Patient is 18 years or over and provides informed consent to participate.
- •2. The patient is aware that recovering from his/her disease is unlikely, as
- •assessed by the attending physician.
- •3. The patient agrees to participate in the iLIVE cohort study.
- •4. The attending physician would not be surprised if the patient were to die
- •within 6 months (*Surprise question*).
- •5. If the physician is uncertain about the surprise question, the patient is
- •eligible if presenting with at least one SPICT indicator.
- •Relatives of included patients are asked to participate if they are:
- •1. 18 years or over and provide informed consent to participate; aware that it
- •is unlikely that the patient will recover from his/her disease;
- •2. capable of filling in a questionnaire in the country*s main language or in
排除标准
- •1. The patient is incapable of filling in a questionnaire in the country*s main
- •language or in English (patients may be supported by relatives when filling in
- •the questionnaire).
- •2. The attending physician makes the decision that the patient should not be
- •included in the study due to e.g. illness burden, fast deterioration or
- •imminent death, lack of trusting relationship with the physician.
- •Relatives are not eligible if they are incapable of filling in a questionnaire
- •in the country*s main language or in English. No more than one relative per
- •patient will be included.
研究者
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