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Tumoren, centraalzenuwstelsel- ×
- Clinical Trial (106)
- Brain Neoplasms (102)
- Treatment Form (25)
- On-Study Form (12)
- Follow-Up Studies (11)
- Eligibility Determination (9)
- Baseline (6)
- Radiotherapy (5)
- Off-Treatment (5)
- Pathology (5)
- Adverse event (4)
- Registration (4)
- Laboratories (3)
- Leukemia (3)
- Quality of Life (2)
- Radiology (2)
- HIV Infections (2)
- Disease Response (2)
- Death (2)
- Questionnaires (1)
- Salvage Therapy (1)
- Disease Notification (1)
- Child (1)
- Symptom Assessment (1)
- Document Tracking (1)
- Drug trial (1)
- Parkinsons Disease (1)
- Demography (1)
- HIV (1)
- Neoplasms (1)
Table des matières
Modèles de données sélectionnés
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106 Résultats de recherche.
Groupes Item: ECG Assessment, CCRR MODULE
Groupes Item: STRATIFICATION, TUMOR LOCATION Elig - Block 1, TUMOR LOCATION Elig - Block 2, INCLUSION CRITERIA - NGGCT STRATUM 1, INCLUSION CRITERIA - Germinoma STRATUM 2, ORGAN FUNCTION REQUIREMENT - Bone Marrow Function, ORGAN FUNCTION REQUIREMENT - Renal Function, ORGAN FUNCTION REQUIREMENT - Liver Function, CENTRAL NERVOUS SYSTEM FUNCTION, EXCLUSION CRITERIA, REGULATORY
Groupes Item: Header Module, SOLID TUMOR/LYMPHOMA ASSESSMENT, KAPOSI'S SARCOMA ASSESSMENT, HEMATOLOGIC MALIGNANCY ASSESSMENT
Groupes Item: Header Module, Patient data, Observation
Groupes Item: Header, Patient characteristics, Concomitant Medication, Patient status, Adverse event
Groupes Item: Header, Eligibility criteria
Groupes Item: Header, Patient characteristics, Treatment, Concomitant Medication, New Cancer, Follow-Up, Adverse event
Groupes Item: Header Module, Summary of Systemic Treatment, Summary of systemic treatment2, Treatment Summary, Protocol Specific Adverse Event Evaluation1, Protocol Specific Adverse Event Evaluation2, Adverse Events, Footer
Groupes Item: Header Module, Summary of Systemic Treatment, Summary of systemic treatment2, Treatment Summary, Protocol Specific Adverse Event Evaluation1, Protocol Specific Adverse Event Evaluation2, Adverse Events, Footer Module
Groupes Item: Header Module, Header, Required Adverse Events from Section 10.0 of Protocol, Adverse Events beyond those required in Section 10.0 of Protocol
Groupes Item: Header Module, Header, Required Adverse Events from Section 10.0 of Protocol, Adverse Events beyond those required in Section 10.0 of Protocol
Groupes Item: Header, Patient Status Information, Events of Interest, CCRR MODULE