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临床试验/ACTRN12617000166370
ACTRN12617000166370已完成未知

Efficacy of early referral to palliative care for improving quality of life and health care resources following recent diagnosis of advanced thoracic maglignancies.

niversity of Sydney0 个研究点目标入组 113 人开始时间: 2017年1月31日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
113

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
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1.Adults, aged 18 years and older, with a histological or cytological diagnosis within the last 60 days of either:
  • (a)Advanced NSCLC (this includes de novo stage IV disease, recurrent NSCLC after definitive treatment, and locally advanced disease which is not planned for curative resection). Patients planned to receive curative intent chemoradiation for locally advanced disease are eligible or
  • (b)Advanced SCLC (this includes extensive stage SCLC, recurrent SCLC after definitive treatment and locally advanced disease), or
  • (c)Advanced MPM which is not planned for extrapleural pneumonectomy or pleurectomy-decortication.
  • 2.Australia-modified Karnofsky performance status of 50 to 100 at the time of randomisation (see Appendix 1).
  • 3.Willing and able to comply with all study requirements, including ability at the time of screening to complete the QOL questionnaires without assistance, in accordance with protocol requirements.
  • 4. Signed, written informed consent.

排除标准

  • 1. Immediate referral to palliative care required, or already referred to palliative care (this
  • includes referral to a community or hospital based palliative care service, or palliative care
  • physician).
  • 2. Life expectancy of less than 3 months.
  • 3. Serious medical or psychiatric onditions that might limit the ability of the patient to comply with the protocol.

研究者

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