Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
24 participants
OBSERVATIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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DEFINED_POPULATION
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patient undergoing with anti-neoplastic agent(s) known to have genotoxic activity (e.g., cyclophosphamide, 5-FU, cisplatin, Ara-C.
* X-irradiation may be considered, so long as a substantial fraction of red marrow is exposed (e.g., femur or chest/trunk region);
* treatment could be ongoing therapy or initial therapy.
21 Years
70 Years
ALL
No
Sponsors
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Litron Laboratories
INDUSTRY
University of Rochester
OTHER
Principal Investigators
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Yuhchyau Chen, MD, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Universtiy of Rochester, Dept of Radiation Oncology
Locations
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University of Rochester
Rochester, New York, United States
Countries
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Other Identifiers
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URCC 1702
Identifier Type: -
Identifier Source: org_study_id