- 04-08-15 - 1 Formulier, 11 Itemgroepen, 85 Data-elementen, 1 Taal
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
- 08-07-15 - 1 Formulier, 18 Itemgroepen, 108 Data-elementen, 1 Taal
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
- 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

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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