跳至主要内容
临床试验/ACTRN12620000271909
ACTRN12620000271909尚未招募未知

Geriatric assessment of frailty in patients with Haematological Malignancies - A study determining the impact of frailty in older people with haematological malignancies.

Dr Angela Molga0 个研究点目标入组 100 人开始时间: 2020年3月2日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
100

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
Open (masking not used)

入排标准

年龄范围
65 Years 至 o limit(—)
性别
All

入选标准

  • Patients must satisfy the following criteria to be enrolled in the study:
  • ·Age 65 years or older
  • ·Diagnosis of haematological malignancy according to relevant classification system
  • oLymphoma –diffuse B-cell lymphoma (DLBCL)
  • oMultiple myeloma – for first line treatment or first relapse
  • oMyelodysplastic syndrome (MDS) and acute myeloid leukemia (AML)
  • ·Ability to provide informed consent. If patients are from a non-english speaking background, informed consent will be determined using an interpreter and including carers
  • ·Able to participate in study assessments
  • ·Life expectancy predicted by the clinician to be over 6 months
  • ·If therapy has commenced at the time of enrollment, then baseline assessments must be completed within 7 days of commencement of therapy

排除标准

  • ·Age <65 years of age
  • ·MDS, AML patients previously treated with azacitidine, intensive chemotherapy and/or allogeneic stem cell transplantation
  • ·DLBCL and multiple myeloma patients failed 2 lines of treatment
  • ·End of life care at time of enrollment
  • ·Best supportive care treatment at time of enrollment. Patients can be reconsented if they are then determined for active therapy and meet all other inclusion criteria.
  • ·Enrollment on any other study where non-interventional studies are prohibited
  • ·Any significant condition that would confound the collection or interpretation of data from the study
  • ·Unable or unwilling to provide consent

研究者

发起方
Dr Angela Molga

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