- 20-09-21 - 1 Formulier, 12 Itemgroepen, 102 Data-elementen, 1 Taal
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
- 08-07-15 - 1 Formulier, 12 Itemgroepen, 67 Data-elementen, 1 Taal
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

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial