Symptom-Related Cytokines in Acute Myeloblastic Leukemia and Myelodysplastic Syndrome Patients
Completed
Conditions studied: Myelodysplastic Syndrome, Acute Myeloblastic Leukemia, Leukemia
In brief
Primary Objective: 1\. To assess the self-reported symptoms and the plasma cytokine levels of AML/MDS patients pretransplantation and posttransplantation with allogeneic blood and marrow in order to identify changes in symptoms (or symptom clusters) and changes in cytokines that may be related to the conditioning regimen and/or to the development of GVHD during the 100 days posttransplant. Based on the current literature, both animal and human research, in this study we hypothesize that increases in TNF alpha to be associated with poor appetite, sleep disturbance and fatigue, but not with increases in pain, depression and numbness.
Key facts
- Study ID
- NCT00504920
- Run by
- M.D. Anderson Cancer Center
- People needed
- 30
- Starts
- 2004-05-01
- Expected to finish
- 2008-09-01
- Last updated by the study team
- 2012-08-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients scheduled for allogeneic transplantation (bone marrow or peripheral blood stem cell) at MDACC.
- Adults > = 18 years old.
- Patients with a diagnosis of AML or MDS
- Patients who are English-speaking
- Patients who live in the United States
- Patients with adequate vision and hearing to use the interactive voice response (IVR) telephone system
- Patients who provide written informed consent/authorization
You may not qualify if…
- Patients with a current diagnosis of psychosis or dementia
- Patients who are unable to complete the assessment measures or refuse to participate
Where it is running
- U.T.M.D. Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.