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Efficacy Study of Tempol to Prevent Hair Loss From Radiotherapy to the Brain - NCT00801086-85724(Clinical Trial 257081)



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City:  Tucson
State:  
AZ
Zip Code: 85724
Conditions: Alopecia
Purpose: Hair loss occurs commonly as a result of radiotherapy administered to the brain, and this can contribute to the distress and social isolation of patients with advanced cancer. In this study a topical gel will be applied directly to the scalp during each dose of radiotherapy. The goal is to determine to what extent the experimental drug is successful in lessening the hair loss.
Study summary:
Criteria: Inclusion Criteria: - Metastatic cancer to the brain for which palliative whole brain radiotherapy is recommended. - Hair that covers the scalp and is at least 1/4 inch in length Exclusion Criteria: - Receiving chemotherapy known to cause alopecia within 60 days of study or during the study. - Pre-existing alopecia - Previous brain radiotherapy - scalp metastases or scalp wounds - use of hair dyes
Study is available at: University of Arizona
Tucson, AZ 85724
United States

Primary Contact:
Jamie Holt
Phone: 520-694-6000
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 22, 2011
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