Inglês

Study Drug Administration A Study of Erlotinib (Tarceva) After Surgery With or Without Adjuvant Chemotherapy in Non-Small Cell Lung Carcinoma (NSCLC) Patients Who Have Epidermal Growth Factor Receptor (EGFR) Positive Tumors (RADIANT) NCT00373425

1 Formulários  
Header
Descrição

Header

Site Number
Descrição

Site number

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C0018704
UMLS CUI [1,2]
C0600091
Patient Number
Descrição

patient number

Tipo de dados

integer

Alias
UMLS CUI [1]
C1830427
Study Drug Administration
Descrição

Study Drug Administration

Start Date
Descrição

Study Drug Administration Start Date

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
Administered Dose
Descrição

Dose

Tipo de dados

float

Unidades de medida
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Stop Date
Descrição

Study Drug Administration Stop Date

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Dose Modification (Record toxicities on the Adverse Events page.)
Descrição

Study Drug Dose Modification

Tipo de dados

integer

Alias
UMLS CUI [1]
C1707811
If other, specify:
Descrição

Study Drug Dose Modification

Tipo de dados

text

Alias
UMLS CUI [1]
C1707811
Missed Doses (Record the number of missed doses, if any, for the time between the start and stop dates.)
Descrição

Missed Doses

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0750480
Voltar ao início da página

Similar models

Study Drug Administration A Study of Erlotinib (Tarceva) After Surgery With or Without Adjuvant Chemotherapy in Non-Small Cell Lung Carcinoma (NSCLC) Patients Who Have Epidermal Growth Factor Receptor (EGFR) Positive Tumors (RADIANT) NCT00373425

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Header
Site number
Item
Site Number
integer
C0018704 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
patient number
Item
Patient Number
integer
C1830427 (UMLS CUI [1])
Item Group
Study Drug Administration
Study Drug Administration Start Date
Item
Start Date
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Dose
Item
Administered Dose
float
C0178602 (UMLS CUI [1])
Study Drug Administration Stop Date
Item
Stop Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Dose Modification (Record toxicities on the Adverse Events page.)
integer
C1707811 (UMLS CUI [1])
Study Drug Dose Modification
Code List
Dose Modification (Record toxicities on the Adverse Events page.)
CL Item
Drug-related Toxicity (AE) (1)
CL Item
Nondrug-related Toxicity (AE) (2)
CL Item
Patient Request  (3)
CL Item
Toxicity lmproved  (4)
CL Item
No Modification (5)
CL Item
Other (specify) (6)
Study Drug Dose Modification
Item
If other, specify:
text
C1707811 (UMLS CUI [1])
Missed Doses
Item
Missed Doses (Record the number of missed doses, if any, for the time between the start and stop dates.)
integer
C1709043 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Voltar ao início da página