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- Clinical Trial (16)
- Follow-Up Studies (14)
- Central Nervous System Neoplasms (13)
- Questionnaires (1)
- Survival (1)
- Breast Neoplasms (1)
- Off-Treatment (1)
- Gynecology (1)
- Neoplasm Metastasis (1)
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16 Resultados de la búsqueda.
Itemgroups: CRF Header, Brain: Vital Status, Brain: Off Study Reason, Brain: Disease Follow-Up Status, Brain: Notice of Progression, Brain: Notice of New Primary, Brain: Long-Term Toxicity
Itemgroups: Header, Patient characteristics, Concomitant Medication, Patient status, Adverse event
Itemgroups: CRF Header, Brain: Follow-up Form Administration, Brain: Baseline Status, Brain: Measurable Lesion(s) Follow-up Evaluation, Brain: Non-measureable/evaluable Lesion(s) Follow-up Evaluation, Brain: New Lesion(s) at Follow-up Evaluation, Brain: Evaluation Summary, Comments
Itemgroups: Date of visit, Assessment Date, follow-up, Continuance of life
Itemgroups: Header, FOLLOW-UP STUDIES, DISEASE STATUS, EVALUATIONS, SIGNIFICANT EVENTS DURING THIS REPORTING PERIOD, CCRR MODULE
Itemgroups: Header Module, Header, Section I - Vital Status, Section II - Reporting Period, Section III - Notice of New Primary, Section IV - Disease Follow-up Status, Section V - Adverse Events, Section VI - Non-Protocol Therapy Prior To (CNS) Progression, Footer Module
Itemgroups: Clinical trial administrative data, Assessment, Disease Progression, Non-Protocol Therapy, Non-Protocol Therapy To Brain, Footer
Itemgroups: Header Module, Header, ON TREATMENT, OFF TREATMENT, Section I, Section II MEASURABLE LESIONS, T2/FLAIR, T1/Contrast, Section III - Lesions Reported as Non-Measurable at Baseline, T2/FLAIR , T1/Contrast, Section IV New CNS Lesions/New Enhancement of Previously Reported Lesions, T2/FLAIR, T1/Contrast, Section V Progression, Comments
Itemgroups: RTOG clinical trial administrative data, Patient status assessment, RECURRENCE OR PROGRESSION, Non-Protocol Therapy, Protocol Specific Adverse Event Evaluation1, Protocol Specific Adverse Event Evaluation2, Comments
Itemgroups: Header, Header
Itemgroups: Header, Patient Status Information, Events of Interest, CCRR MODULE
Itemgroups: Header, Secondary Malignancy, CCRR MODULE