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Keywords
Brain Neoplasms ×
- Clinical Trial (126)
- Central Nervous System Neoplasms (102)
- Treatment Form (30)
- On-Study Form (14)
- Follow-Up Studies (14)
- Eligibility Determination (12)
- Neoplasm Metastasis (12)
- Breast Neoplasms (9)
- Gynecology (8)
- Baseline (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)
- Medical Oncology (2)
- Neurologic Examination (2)
- Pharmacogenetics (1)
- Pregnancy (1)
- Questionnaires (1)
- Survival (1)
- Salvage Therapy (1)
- Disease Notification (1)
- Vital Signs (1)
- Child (1)
- Symptom Assessment (1)
- Concomitant Medication (1)
- Document Tracking (1)
- End of Study (1)
- Routine documentation (1)
- Demography (1)
- HIV (1)
- Neurology (1)
- Pediatrics (1)
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130 Search results.
Itemgroup: Pediatric oncology brain tumor tumor board request
Itemgroups: Header,Eligibility criteria
Itemgroups: Date of visit, Assessment Date,Neurologic Examination,Neurologic Symptoms, Associated with, Neoplasms,Laboratory Procedures, Central Laboratory; Laboratory Procedures, Local,Laboratory Procedures, Chemistry, Clinical,Laboratory Procedures, Hematology finding,Central Laboratory, Data,Vital signs,Continuation status, Study
Itemgroups: Date of visit, Assessment Date,Neurologic Examination,Neurologic Symptoms, Associated with, Neoplasms,Vital signs,Randomization, Numbers,Therapeutic regimen
Itemgroups: Header,Patient characteristics,Concomitant Medication,Patient status,Adverse event
Itemgroups: Header,I. CRA/RN,II. Completed by the NCCTG Pathology reviewer,Comments and Pathology Reporting
Itemgroups: Date of visit, Assessment Date,Event Log, Status,Non-serious Adverse Event,Serious Adverse Event,Concomitant Agent,Concomitant Agent, Adrenal Cortex Hormones,Blood product; Supportive care,Collection of blood specimen for laboratory procedure, Pharmacogenetic Test, Informed Consent,Pharmacogenetic Test, Informed Consent, Withdraw (activity)
Itemgroups: Inclusion Criteria,Exclusion Criteria
Itemgroups: Date of visit, Assessment Date,Laboratory Procedures, Central Laboratory; Laboratory Procedures, Local,Laboratory Procedures, Chemistry, Clinical,Laboratory Procedures, Hematology finding,Central Laboratory, Data,Disease, Operative Surgical Procedures,Vital signs,Experimental drug, Topotecan, Dosage,Therapeutic procedure, Confirmation,Lapatinib, Compliance behavior,Continuation status, Study
Itemgroups: Date of visit, Assessment Date,Laboratory Procedures, Central Laboratory; Laboratory Procedures, Local,Laboratory Procedures, Chemistry, Clinical,Laboratory Procedures, Hematology finding,Central Laboratory, Data,Vital signs,Experimental drug, Topotecan, Dosage,Therapeutic procedure, Confirmation,Lapatinib, Compliance behavior,Continuation status, Study
Itemgroups: Date of visit, Assessment Date,Visit, Previous,Laboratory Procedures, Central Laboratory; Laboratory Procedures, Local,Laboratory Procedures, Chemistry, Clinical,Laboratory Procedures, Hematology finding,Central Laboratory, Data,Vital signs,Experimental drug, Lapatinib,Experimental drug, Topotecan, Dosage,Therapeutic procedure, Confirmation,Lapatinib, Compliance behavior,Continuation status, Study
Itemgroups: Date of visit, Assessment Date,Cessation of life,Pregnancy, Information,Conclusion, Clinical Research