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Neoplasia ×
- Urinary Bladder Neoplasms (27)
- Clinical Trial (26)
- Eligibility Determination (6)
- Follow-Up Studies (4)
- Breast Neoplasms (3)
- On-Study Form (3)
- Treatment Form (3)
- Prostatic Neoplasms (2)
- Skin Neoplasms (2)
- Peritoneal Neoplasms (1)
- Pheochromocytoma (1)
- Adenomatous Polyposis Coli (1)
- Questionnaires (1)
- Testicular Neoplasms (1)
- Thoracic Neoplasms (1)
- Thyroid Neoplasms (1)
- Urogenital Neoplasms (1)
- Vulvar Neoplasms (1)
- Lymphoma, Large B-Cell, Diffuse (1)
- Bile Duct Neoplasms (1)
- Endometrial Neoplasms (1)
- Adrenocortical Carcinoma (1)
- Cholangiocarcinoma (1)
- Hemangioblastoma (1)
- Urothelium (1)
- Brain Neoplasms (1)
- Carcinoma, Renal Cell (1)
- Chemistry (1)
- Adverse event (1)
- Registration (1)
- Pre-Study Form (1)
- Off-Treatment (1)
- Colonic Neoplasms (1)
- Colonic Polyps (1)
- Cystoscopy (1)
- Digestive System Neoplasms (1)
- Endocrine Gland Neoplasms (1)
- Esophageal Neoplasms (1)
- Fallopian Tube Neoplasms (1)
- Glioblastoma (1)
- Head and Neck Neoplasms (1)
- Hematologic Tests (1)
- Hyperparathyroidism (1)
- Kidney Neoplasms (1)
- Laboratories (1)
- Leiomyoma (1)
- Liver Neoplasms (1)
- Lung Neoplasms (1)
- Melanoma (1)
- Mouth Neoplasms (1)
- Abdominal Neoplasms (1)
- Nervous System Neoplasms (1)
- Ovarian Neoplasms (1)
- Pancreatic Neoplasms (1)
- Paraganglioma (1)
- Pathology (1)
Inhoudsopgave
Geselecteerde datamodellen
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30 Zoekresultaten.
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Header Module, Treatment Information, Off Treatment Reason, Additional Treatment, Vital Status
Itemgroepen: Inclusion criteria, Exclusion criteria
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Header, Vital Status, Treatment Status, Disease Assessment, Measurable Disease Response, Notice of New Primary, Long-Term Toxicity, Non-Protocol Therapy
Itemgroepen: Muscle Invasive Bladder Disease: Prior Treatment Affecting the Bladder, Prior Therapy Date, CCRR MODULE
Itemgroepen: Administrative documentation, Hematology finding
Itemgroep: CCRR MODULE
Itemgroepen: Header, Urine Markers, Cytoscopy, Comments
Itemgroepen: Header Module, Adverse Events, Comments
Itemgroep: CCRR MODULE
Itemgroepen: Protocol Information, SWOG PATIENT ID, DEMOGRAPHY, For SWOG Institutions:, Patient Information, Indicate how the patient answered the following questions on the consent form, Patient Eligibility