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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)
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- Prostatic Neoplasms (1)
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- Therapeutics (1)
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- Urogenital Neoplasms (1)
- Colorectal Neoplasms (1)
- Pulmonary Medicine (1)
- Clinical Trial, Phase II (1)
- Breast Neoplasms (1)
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Itemgroepen: Header, Head and Neck cancer characteristics
Itemgroep: MODULE 1
Itemgroepen: Header, Vital Status, Treatment
Itemgroepen: Header, Patient demographics, PRIOR TREATMENT, COMORBIDITY, DIAGNOSTIC WORK-UP, LABORATORY TESTS, TUMOR MEASUREMENTS AT PRESENTATION, Protocol Specific Adverse Event Evaluation, COMMENTS
Itemgroepen: Header Module, Patient demographics, Swallowing problems/Smoking history, DIAGNOSTIC WORK-UP, Laboratory Values, Primary Site, Staging, Surgery and Pathologic Risk Factors, PRIOR TREATMENT, SEVERE ACTIVE COMORBIDITIES, Protocol Specific Adverse Event Evaluation, Footer Module
Itemgroepen: Header, Unnamed3, Unnamed2, TARGET LESIONS, NONTARGET LESIONS, Comments
Itemgroepen: Patient Information 1, Patient Information
Itemgroep: Radiotherapy Form
Itemgroepen: Header Module, Demographic Data, Cigarette History, Family History
Itemgroepen: Header Module, SUMMARY OF SYSTEMIC TREATMENT, WEEK 1-INITIAL DOSE, WEEK 2, WEEK 3, WEEK 4, WEEK 5, WEEK 6, WEEK 7, WEEK 8, WEEK 9, WEEK 10, WEEK 11, Header, Footer Module
Itemgroepen: Header Module, QOL Cover Sheet, Health Utility Measurement, Header
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