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Keywords
Head and Neck Neoplasms ×
- 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)
- EHR (1)
- Off-Treatment (1)
- Document Tracking (1)
- Recurrent Squamous Cell Carcinoma (1)
- Dermatology (1)
- Digestive System Neoplasms (1)
- Endocrine Gland Neoplasms (1)
- Hospitals, University (1)
- Hypopharyngeal Neoplasms (1)
- Laboratories (1)
- Mouth Neoplasms (1)
- Nasopharyngeal Neoplasms (1)
- Neoplasms (1)
- Neoplasms, Unknown Primary (1)
- Abdominal Neoplasms (1)
- Nervous System Neoplasms (1)
- Antineoplastic Agents (1)
- Otorhinolaryngologic Diseases (1)
- Ovarian Neoplasms (1)
- Palliative Care (1)
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124 Search results.
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroup: Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroup: pht005773
pht005774.v1.p1
1 itemgroup 5 itemspht005775.v1.p1
1 itemgroup 8 itemsEligibility
1 itemgroup 1 itempht005776.v1.p1
1 itemgroup 6 items Itemgroups: Inclusion Criteria, Exclusion Criteria
Head and Neck Cancer NCT00265941 Follow-Up - Follow-up Head and Neck Cancer RTOG-0522 F1 NCT00265941
Itemgroups: Header, CURRENT DISEASE STATUS AND METHOD OF DETERMINATION, DISEASE EVENTS, New primary cancer, Non-Protocol Therapy, Swallowing and Tube Feeding, Protocol Specific Adverse Event Evaluation, Other Adverse Events
Itemgroups: Inclusion Criteria, Exclusion Criteria
Itemgroups: 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
Itemgroups: Header, COMMENTS