- 08/07/2015 - 1 Formulário, 12 Grupos de itens, 70 Elementos de dados, 1 Idioma
Grupos de itens: RTOG clinical trial administrative data, Summary of Concurrent Treatment, Treatment Summary, Therapy Modification, Toxicities, PROTOCOL SPECIFIC ADVERSE EVENT EVALUATION, PROTOCOL SPECIFIC ADVERSE EVENT EVALUATION DAY 8, PROTOCOL SPECIFIC ADVERSE EVENT EVALUATION DAY 15, PROTOCOL SPECIFIC ADVERSE EVENT EVALUATION DAY 22, PROTOCOL SPECIFIC ADVERSE EVENT EVALUATION DAY 29, Adverse Events, Comments
- 09/01/2015 - 1 Formulário, 6 Grupos de itens, 15 Elementos de dados, 1 Idioma
Grupos de itens: Protocol Administration, Pre-Treatment Characteristics, Certification Of Eligibility, Protocol Design (Stratification Factors), Companion Studies - Study 151007: Molecular Markers of Treatment Response (optional), Companion Studies - Study 71003: Correlation of QOL with Treatment Response and Validation of PRO-CTCAE (optional)

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