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- Clinical Trial (113)
- Eligibility Determination (45)
- Otolaryngology (29)
- Quality of Life (18)
- Treatment Form (17)
- On-Study Form (10)
- Follow-Up Studies (9)
- Oropharyngeal Neoplasms (7)
- Carcinoma, Squamous Cell (6)
- Baseline (4)
- Demography (4)
- Neoplasms, Squamous Cell (3)
- Registration (3)
- Non Small Cell Lung Cancer (3)
- Radiology (2)
- Adverse event (2)
- Routine documentation (2)
- Medical Oncology (2)
- Appendix (1)
- Pharyngeal Neoplasms (1)
- Prostatic Neoplasms (1)
- Skin Neoplasms (1)
- Therapeutics (1)
- Thoracic Neoplasms (1)
- Urogenital Neoplasms (1)
- Colorectal Neoplasms (1)
- Pulmonary Medicine (1)
- Clinical Trial, Phase II (1)
- Breast Neoplasms (1)
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- Recurrent Squamous Cell Carcinoma (1)
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- Nervous System Neoplasms (1)
- Antineoplastic Agents (1)
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Geselecteerde datamodellen
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124 Zoekresultaten.
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Inclusion Criteria, Exclusion Criteria
Itemgroepen: Header Module, Patient demographics, Tumor Measurements At Presentation, Basis of Diagnosis, Laboratory Values, Primary Site, Staging, PRIOR TREATMENT, SEVERE ACTIVE COMORBIDITIES, Protocol Specific Adverse Event Evaluation: Use the CTC AE version 4 (MedDRA 12) to code all events., Footer Module
Itemgroepen: RTOG clinical trial administrative data, SUMMARY OF SYSTEMIC TREATMENT, INITIAL DOSE, WEEK 1 - DAY 1 - ACTUAL, WEEK 1 - DAY 1 - IDEAL, WEEK 2, WEEK 3, WEEK 4 - ACTUAL, WEEK 4 - IDEAL, WEEK 5, WEEK 6, WEEK 7, Off-protocol treatment, Protocol Specific Adverse Event Evaluation, Other Adverse Events, Lab Values Module, Make up doses #1-4, Comments
Itemgroepen: RTOG clinical trial administrative data, Summary of Systemic Treatment, ARM 1 ONLY - DAY 1, DAY 22, Header, ARM 2 ONLY - WEEK 1 - INITIAL DOSE, WEEK 2-8, Non-Protocol Therapy, Tube feeding, Protocol Specific Adverse Event Evaluation: Use the CTC AE version 4 (MedDRA 12) to code all events., New or continuing adverse events, Comments
Itemgroepen: RTOG clinical trial administrative data, Various questionnaire related information
Itemgroepen: RTOG clinical trial administrative data, REPORT ALL CONTINUING OR NEW ADVERSE EVENTS
Itemgroepen: RTOG clinical trial administrative data, REPORT ALL CONTINUING OR NEW ADVERSE EVENTS
Itemgroepen: Header Module, Vital status, Tumor Measurements At Presentation, RECURRENCE OR PROGRESSION, New primary cancer, NON-PROTOCOL THERAPY, Protocol Specific Adverse Event Evaluation, New or continuing adverse events, Comments