Skip to main content
Clinical Trials/ACTRN12620000271909
ACTRN12620000271909
Not yet recruiting
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 sites100 target enrollmentMarch 2, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Frailty
Sponsor
Dr Angela Molga
Enrollment
100
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 2, 2020
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Angela Molga

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • ·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

Outcomes

Primary Outcomes

Not specified

Similar Trials