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Primary Malignant Brain Neoplasms ×
- Clinical Trial (126)
- Central Nervous System Neoplasms (102)
- Treatment Form (30)
- On-Study Form (14)
- Follow-Up Studies (14)
- Eligibility Determination (11)
- Neoplasm Metastasis (11)
- Breast Neoplasms (8)
- Baseline (7)
- Gynecology (7)
- Adverse event (6)
- Laboratories (6)
- Radiotherapy (5)
- Off-Treatment (5)
- Drug trial (5)
- Pathology (5)
- Registration (4)
- Death (3)
- Leukemia (3)
- Quality of Life (2)
- Radiology (2)
- HIV Infections (2)
- Disease Response (2)
- Laboratory Infection (2)
- Pharmacogenetics (1)
- Pregnancy (1)
- Questionnaires (1)
- Survival (1)
- Salvage Therapy (1)
- Disease Notification (1)
- Child (1)
- Symptom Assessment (1)
- Concomitant Medication (1)
- Document Tracking (1)
- End of Study (1)
- Demography (1)
- HIV (1)
- Medical Oncology (1)
- Neurologic Examination (1)
- Neurology (1)
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Geselecteerde datamodellen
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126 Zoekresultaten.
Itemgroepen: 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
Itemgroepen: 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
Itemgroepen: 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
Itemgroepen: Header, Secondary Malignancy, CCRR MODULE
Itemgroepen: Header, Relapse/Progression, CCRR MODULE
Itemgroepen: Header, Death Assessment, Comments, CCRR MODULE
Itemgroepen: Clinical trial administrative data, Assessment, Disease Progression, Non-Protocol Therapy, Non-Protocol Therapy To Brain, Footer
Itemgroepen: Header, FOLLOW-UP STUDIES, DISEASE STATUS, EVALUATIONS, SIGNIFICANT EVENTS DURING THIS REPORTING PERIOD, CCRR MODULE
Itemgroepen: Header, Date of relapse or progression, TYPE OF RECURRENCE/PROGRESSION, SITES OF INVOLVEMENT, Comments, CCRR MODULE
Itemgroepen: Header, Patient characteristics, Concomitant Medication, Patient status, Adverse event
Itemgroepen: Header Module, RECURRENCE OR PROGRESSION, CONTACT INFORMATION FOR TREATING PHYSICIAN, Footer Module
Itemgroepen: 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