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Palliative Transfusions for Blood Cancer (PalliaQOL Trial)
N/A
Waitlist Available
Led By Jennifer Holter, MD
Research Sponsored by University of Oklahoma
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients wanting to enroll in hospice.
All patients >= 18 years with a primary diagnosis of acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), chronic myelomonocytic leukemia (CMML), 'high risk' Non-Hodgkin's Lymphoma (NHL), multiple myeloma (MM) and Myelodysplastic Syndrome (MDS) with a life expectancy of < 6 months who are transfusion dependent. Criteria for transfusion dependence is Symptom Questionnaire symptom grade 2 or higher. The Symptom Questionnaire is based on CTCAE (Common Terminology Criteria for Adverse Events) v5.0, with criteria modified for palliative care patients.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
PalliaQOL Trial Summary
This trial will study whether blood transfusions can help improve symptoms and quality of life for hospice patients.
Who is the study for?
This trial is for adults over 18 with certain blood cancers like AML, ALL, CLL, CMML, 'high risk' NHL, MM or MDS who need regular transfusions and have less than 6 months to live. They must want hospice care and either have an IV line or agree to get one.Check my eligibility
What is being tested?
The study tests if blood and platelet transfusions can help improve symptoms and life quality for hospice patients with specific blood cancers. It involves regular CBC collections to monitor the impact of these transfusions.See study design
What are the potential side effects?
Potential side effects may include reactions at the infusion site, allergic responses to the transfused blood products, fatigue from the procedure itself, or complications related to having an IV line.
PalliaQOL Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am considering enrolling in hospice care.
Select...
I am 18 or older with a specific blood cancer and need regular blood transfusions.
PalliaQOL Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Proportion of subjects with improved palliative efficacy after receiving transfusions.
Proportion of subjects with improved quality of life after receiving transfusions.
PalliaQOL Trial Design
1Treatment groups
Experimental Treatment
Group I: Tranfusions and blood collectionExperimental Treatment2 Interventions
Patients enrolled will receive one unit each of blood and/or platelet transfusions once a week based on trigger symptoms of anemia and/or thrombocytopenia, along with blood sample collections.
Data on patient demographics, disease, and length of hospice stay will also be collected.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Blood and/or platelet transfusion
2020
N/A
~20
Complete blood count (CBC) collection
2020
N/A
~20
Find a Location
Who is running the clinical trial?
University of OklahomaLead Sponsor
455 Previous Clinical Trials
97,590 Total Patients Enrolled
Jennifer Holter, MDPrincipal InvestigatorUniversity of Oklahoma
2 Previous Clinical Trials
73 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am considering enrolling in hospice care.I am not willing to enter hospice care.I cannot donate blood or platelets due to specific antibodies.I am 18 or older with a specific blood cancer and need regular blood transfusions.
Research Study Groups:
This trial has the following groups:- Group 1: Tranfusions and blood collection
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there still positions available in this clinical trial for volunteers?
"Affirmative. Clinicaltrials.gov verifies that this research project, which was initially posted on August 14th 2020, is now looking for 20 volunteers from one medical centre."
Answered by AI
What is the upper limit of participants for this research endeavor?
"Affirmative. According to clinicaltrials.gov, the trial which was originally publicized on August 14th 2020 is currently recruiting subjects. This study requires 20 participants from a single site."
Answered by AI
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