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Trial Information
Summary: Study of transplantation using umbilical cord and placental blood
This study investigates the concept that umbilical cord blood
stem cells can be used for allogeneic transplant with the same or
better outcome as following a conventional bone marrow
transplant.
Patients must fulfill the following criteria:
- Firm diagnosis by standard clinical and/or pathological
criteria of chronic myeloid leukemia, acute leukemia, lymphoma,
myeloma, myelodysplasia, aplastic anemia, Fanocni's anemia,
histiocytosis, hereditary immunodeficiency, and storage
disorders
- Physiological age < 60 years
- Non pregnant, non lactating
- No other serious medical or psychiatric illness preventing
informed consent or intensive treatment (e.g., serious
infection)
- Consensus agreement that UCB transplantation is appropriate
after discussion at Adult Leukemia/Lymphoma/Hematology conference,
Pediatric Oncology Rounds, Medical Oncology BMT Conference or
Pediatric Hematology Rounds
- Eligible for standard allogeneic BMT but lacking a suitable
marrow or blood stem cell donor.
- Availability of UCB form the NY Blood Center which is
mismatched for 0, 1, or 2 HLA loci, Serological tissue typing for
class I antigens and serological methods or low resolution DNA
testing for class II antigens.
- Availablity of UCB which contains more than or equal to 1x
107 nucleated cells/kg ideal body weight of recipient
and which is seronegative for HIV, hepatitis B5 Ag. and
hepatitis C virus.
- Serum bilirubin < 2x normal and no other evidence of severe
hepatic disease
- Recipient seronegative for HIV, hepatitis B5 Ag. and
hepatitis C virus.
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Contact:
George Nevrodis, Project Coordinator
Columbia-Presbyterian Medical Center
177 Fort Washington Avenue
New York, NY 10032
Telephone: 212-305-0176
Fax: 212-305-0178
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Trial listings updated: June 1, 2008 at 5:43:10 AM
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