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| 1 | Conditions listed in this trial | ||||
| Breast Cancer | |||||
| Cancer-Related Problem/Condition | |||||
| 2 | Additional conditions recognized in this trial | ||||
| Breast Neoplasms | |||||
| Carcinoma in Situ | |||||
| Carcinoma, Intraductal, Noninfiltrating | |||||
| Dermatitis | |||||
| Radiodermatitis | |||||
| 3 | More general conditions related to this trial | ||||
| Adenocarcinoma | |||||
| Breast Diseases | |||||
| Carcinoma | |||||
| Disorders of Environmental Origin | |||||
| Neoplasms | |||||
| Neoplasms by Histologic Type | |||||
| Neoplasms by Site | |||||
| Neoplasms, Ductal, Lobular, and Medullary | |||||
| Neoplasms, Glandular and Epithelial | |||||
| Radiation Injuries | |||||
| Skin Diseases | |||||
| Wounds and Injuries | |||||
| 4 | Interventions listed in this trial | ||||
| mometasone furoate | |||||
| placebo | |||||
| 5 | More general drug interventions related to this trial | ||||
| Anti-Allergic Agents | |||||
| Anti-Inflammatory Agents | |||||
| Pharmacologic Actions | |||||
| Therapeutic Uses | |||||
| 6 | Sponsors listed in this trial | ||||
| North Central Cancer Treatment Group | |||||
| National Cancer Institute (NCI) | |||||