Assessment of Pain in People With Thalassemia Who Are Treated With Regular Blood Transfusions



Status:Completed
Conditions:Hematology
Therapuetic Areas:Hematology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:July 2009
End Date:October 2010

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Assessment of Pain in Transfusion Dependent Patients With Thalassemia During Transfusion Cycles

Thalassemia is an inherited blood disorder that can result in mild to severe anemia. Regular
blood transfusions, which refresh the healthy red blood cell supply, are one treatment for
thalassemia. People with thalassemia often experience pain, but the exact source of pain
remains unknown. This study will examine how pain varies during the blood transfusion cycle
in people with thalassemia who are treated with regular blood transfusions.

Thalassemia is an inherited blood disorder in which the body makes an abnormal form of
hemoglobin—the protein in red blood cells that carries oxygen. People with thalassemia often
experience fatigue, shortness of breath, and pain. There have been no previous research
studies that have fully examined pain levels in people with thalassemia, and as a result,
the sources of pain remain unknown. This study is a substudy of the Assessment of Pain
study, which is a Thalassemia Clinical Research Network (TCRN) study that is examining the
prevalence and severity of pain in people with transfusion-dependent thalassemia and
non-transfusion-dependant thalassemia. This study will enroll a subset of participants from
the Assessment of Pain study who have transfusion-dependant thalassemia. The purpose of this
study is to examine whether pain varies during the blood transfusion cycle and whether the
length of the transfusion cycle affects pain levels in people with transfusion-dependent
thalassemia.

Participants will complete daily questionnaires through an automated telephone system to
assess pain levels during three blood transfusion cycles. Each transfusion cycle will last
between 2 to 4 weeks, depending on the individual needs of the participant, and the cycles
will be separated by at least 3 months but no more than 4 months. Prior to each transfusion
cycle, study researchers will review participants' medical records for certain blood level
measurements.

Inclusion Criteria:

- Participating in the Thalassemia Clinical Research Network Assessment of Pain study

- Has a transfusion dependence of at least eight transfusions per year

- Diagnosis of beta thalassemia or E-beta-thalassemia

- Experiences at least "mild" pain in the 1 month before study entry, as measured by
the response to the Brief Pain Inventory (BPI) question #6 from the Assessment of
Pain study

Exclusion Criteria:

- Unwillingness or inability to complete the Brief Pain Inventory Short Form (BPI-SF)
on a daily basis
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1200 Moursund Street
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South 34th Street
Philadelphia, Pennsylvania 19104
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291 Campus Dr
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Atlanta, Georgia 30322
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Chicago, Illinois 60614
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New York, New York 10021
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