ISRCTN10644347已完成未知
A single arm observational SYmptom Study of radioThErapy in MeSothelioma
HS Greater Glasgow and Clyde (UK)0 个研究点目标入组 40 人开始时间: 2012年8月3日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 40
研究概览
简要总结
2015 Results article in http://www.ncbi.nlm.nih.gov/pubmed/25654216 results 2016 Results article in http://www.ncbi.nlm.nih.gov/pubmed/27117437 results
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •1. >/=18 years of age.
- •2. Histological or multi-disciplinary team (MDT) diagnosis of mesothelioma
- •3. Able to complete study assessments
- •3. Life expectancy of at least 3 months based on clinical judgement
- •4. Due to receive radiotherapy for pain resulting from mesothelioma (defined as index site ? site of radiotherapy)
- •5. Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2
- •6. CT scan within 6 weeks of radiotherapy
- •7. Worst pain >4/10 (0-10 Visual Analogue Scale) corresponding to the index site
排除标准
- •1. Received chemotherapy or radiotherapy in the preceding six weeks that is likely to alter pain at the index site during the duration of the study
- •2. Planned chemotherapy during the period of the study that is likely to alter pain during the course of the study
- •3. Psychotic disorders or cognitive impairment
- •4. Co-existing lung tumours at the time of study entry
- •5. Pregnant or breastfeeding
研究者
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