ACTRN12620000842965撤回3 期
COVID-19 Prevention and Treatment in Cancer; a Sequential Multiple Assignment Randomised Trial; C-SMART study.Arm 2: Effect of daily Interferon-alpha on cancer patients with known positive contact with COVID-19.
Peter MacCallum Cancer Centre0 个研究点目标入组 170 人开始时间: 2020年8月26日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 撤回
- 发起方
- 入组人数
- 170
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
- Prevention
- 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. Age equal to or greater than 18 years old.
- •2. Any haematological or solid tumour
- •3. Current or within the last 12 months received cancer related treatment such as chemotherapy, radiotherapy or targeted small molecule, cellular therapy or immune-modulating therapy
- •4. Signed written and verbal informed consent
- •5. Have been exposed to a known COVID-19 case within the last 72 hours, defined by the current Department of Health and Human services such as household contact, 15 minutes of face to face exposure, 2 hours in close space.
- •6. Willingness to inform the study nurse/co-ordinator of COVID-19 testing
- •7. Willingness to perform a self-collect nose/throat swab
排除标准
- •1. Previous diagnosis of COVID-19 (microbiologically proven, either symptomatic or asymptomatic)
- •2. Any contra-indication to intra-nasal IFN-a such as severe nasal bleeding requiring intervention, nasal malignancy, nasal deformity, radiotherapy to the nasopharynx and/or oropharynx
- •3. Pregnant or breast-feeding women, or women who wish to become pregnant during the course of the study
- •4. Patient unable to return for follow-up
- •5. Life expectancy of less than 1 month
- •6. Patient already included in another intervention study on the prevention of COVID-19
- •7. Currently unwell with influenza-like symptoms
研究者
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