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Mots-clés
Tumeurs de l'oro-pharynx ×
- Clinical Trial (10)
- Head and Neck Neoplasms (7)
- Eligibility Determination (4)
- Otolaryngology (4)
- Quality of Life (2)
- Follow-Up Studies (2)
- Hypopharyngeal Neoplasms (2)
- Pharyngeal Neoplasms (1)
- On-Study Form (1)
- Treatment Form (1)
- Laryngeal Neoplasms (1)
- Mouth Neoplasms (1)
Table des matières
Modèles de données sélectionnés
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11 Résultats de recherche.
Groupes Item: Header Module, HEARING HANDICAP INVENTORY FOR ADULTS SCREENING QUESTIONNAIRE (NEWMAENT AL., 1990; NEWMAENT AL., 1991)
Groupe Item: pht005773
pht005774.v1.p1
1 Groupe Item 5 Eléments de donnéespht005775.v1.p1
1 Groupe Item 8 Eléments de donnéesEligibility
1 Groupe Item 1 Élément de donnéespht005776.v1.p1
1 Groupe Item 6 Eléments de données Groupes Item: 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
Groupes Item: Inclusion Criteria, Exclusion Criteria
Groupes Item: Inclusion Criteria, Exclusion Criteria
Groupes Item: Inclusion Criteria, Exclusion Criteria
Groupes Item: Inclusion Criteria, Exclusion Criteria
Groupes Item: 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
Groupes Item: 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
Groupes Item: RTOG clinical trial administrative data, Patient status assessment, RECURRENCE OR PROGRESSION, New primary cancer, Non-protocol Therapy, Protocol Specific Adverse Event Evaluation, New or continuing adverse events, Comments
Groupes Item: Header Module, PRO-CTCAE Assessment, PRO-CTCAE Assessment (cont.1), PRO-CTCAE Assessment (cont.2), PRO-CTCAE Assessment (cont.3) , PRO-CTCAE Assessment (cont.4)