Myelodysplastic Syndrome Clinical Trial

Palliative Care Oncology in Patients With Relapsed, Refractory, and High-Risk Leukemias or MDS

Summary

The purpose of this study is to estimate the potential benefit of early and continued palliative care (PC) consultation on end of life issues.

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Full Description

Participants in this study will be randomized to either an intervention group or a standard of care group. Participants in the intervention group will participate in regular visits with a palliative (or supportive) care specialist, while participants in the standard of care group will only see palliative care specialists if the clinician requests a referral. All participants will be asked to complete monthly questionnaires regarding their general well-being.

Participants have a greater chance of being assigned to the intervention group than to the standard of care group. On average, in every 5 people randomized, 3 will be randomized to the intervention and 2 will be randomized to standard of care.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Ability to provide informed consent
Stated willingness to comply with all study procedures and availability for the duration of the study

Any of the following:

Patients with a new diagnosis of AML, ALL, high risk myelodysplastic syndrome (MDS), or high risk chronic myelomonocytic leukemia (CMML) who are age 65 and older.

OR

Patients with relapsed AML, ALL, high risk MDS or high risk CMML, ages 18 and older.

OR

Patients with refractory AML, ALL, high risk MDS or high risk CMML, ages 18 and older.

Refractory AML/ALL will be defined as persistent leukemia despite two or more cycles of induction chemotherapy.

Refractory MDS will be defined according to the 2006 IWG response criteria Refractory CMML will be based on the assessment of the treating investigator.

Exclusion Criteria:

1. Participants must not have a diagnosis of Acute Promyelocytic Leukemia (APL)

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

105

Study ID:

NCT04482894

Recruitment Status:

Recruiting

Sponsor:

University of Virginia

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There is 1 Location for this study

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University of Virginia
Charlottesville Virginia, 22903, United States More Info
Emily Leytham
Contact
434-924-7621
[email protected]
Emily Hoade
Contact
(434) 243-3983
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

105

Study ID:

NCT04482894

Recruitment Status:

Recruiting

Sponsor:


University of Virginia

How clear is this clinincal trial information?

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