Dosing regime - GSK Study: GW679769 administered alone vs. with dexamethasone - Evaluation of safety, tolerability and pharmacokinetics NCT00291876

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StudyEvent: ODM
1. Dosing regime - GSK Study: GW679769 administered alone vs. with dexamethasone - Evaluation of safety, tolerability and pharmacokinetics NCT00291876

Regime selection

Descripción

Regime selection

Alias

UMLS CUI-1: C0013153

UMLS CUI-2: C0679006

Please select a regime for this subject and this session and press "continue".

Descripción

drug administration regime decision

Tipo de datos

integer

Alias

UMLS CUI [1,1]: C0013153

UMLS CUI [1,2]: C0679006

O-Single 150mg Oral of GW679769 (1)

P-Placebo for IV GW679769 (2)

X1-IV GW679769 12mg (3)

X2-IV GW679769 12-35mg (4)

X3-IV GW679769 35-70mg (5)

X4-IV GW679769 70-130mg (6)

Study medication oral

Descripción

Study medication oral

Alias

UMLS CUI-1: C0013227

UMLS CUI-2: C0304229

UMLS CUI-3: C1527415

Session day

Descripción

Dosing day

Tipo de datos

partialDate

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439228

Session hour

Descripción

Session hour

Tipo de datos

partialDatetime

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439227

Session minute

Descripción

Session minute

Tipo de datos

partialDatetime

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439232

Start Dose Date

Descripción

Start dose date

Tipo de datos

date

Alias

UMLS CUI [1,1]: C0808070

UMLS CUI [1,2]: C0178602

Start Dose Time

Descripción

Start dose time

Tipo de datos

time

Alias

UMLS CUI [1,1]: C1301880

UMLS CUI [1,2]: C0178602

Dose amount

Descripción

Dose amount

Tipo de datos

integer

Alias

UMLS CUI [1,1]: C0178602

UMLS CUI [1,2]: C1264637

Dose units

Descripción

Dose unit

Tipo de datos

text

Alias

UMLS CUI [1]: C0869039

Dose formulation

Descripción

Dose form

Tipo de datos

text

Alias

UMLS CUI [1]: C0013058

Dose route

Descripción

Dose route

Tipo de datos

text

Alias

UMLS CUI [1,1]: C0013153

UMLS CUI [1,2]: C0679006

Study Medication IV

Descripción

Study Medication IV

Alias

UMLS CUI-1: C0013227

UMLS CUI-2: C0304229

UMLS CUI-3: C1522726

Session day

Descripción

Dosing day

Tipo de datos

partialDate

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439228

Session hour

Descripción

Session hour

Tipo de datos

partialDatetime

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439227

Session minute

Descripción

Session minute

Tipo de datos

partialDatetime

Alias

UMLS CUI [1,1]: C1883016

UMLS CUI [1,2]: C0439232

Start Dose Date

Descripción

Start dose date

Tipo de datos

date

Alias

UMLS CUI [1,1]: C0808070

UMLS CUI [1,2]: C0178602

Start Dose Time

Descripción

Start dose time

Tipo de datos

time

Alias

UMLS CUI [1,1]: C1301880

UMLS CUI [1,2]: C0178602

End Dose Date

Descripción

End Dose Date

Tipo de datos

date

Alias

UMLS CUI [1,1]: C0806020

UMLS CUI [1,2]: C0178602

End Dose Time

Descripción

End Dose Time

Tipo de datos

time

Alias

UMLS CUI [1,1]: C1522314

UMLS CUI [1,2]: C0178602

Start Dose Volume

Descripción

Start Dose Volume

Tipo de datos

text

Alias

UMLS CUI [1,1]: C0449468

UMLS CUI [1,2]: C0178602

UMLS CUI [1,3]: C0439659

End Dose Volume

Descripción

End Dose Volume

Tipo de datos

text

Alias

UMLS CUI [1,1]: C0449468

UMLS CUI [1,2]: C0178602

UMLS CUI [1,3]: C0444930

Dose amount

Descripción

Dose amount

Tipo de datos

integer

Alias

UMLS CUI [1,1]: C0178602

UMLS CUI [1,2]: C1264637

Dose units

Descripción

Dose unit

Tipo de datos

text

Alias

UMLS CUI [1]: C0869039

Dose formulation

Descripción

Dose form

Tipo de datos

text

Alias

UMLS CUI [1]: C0013058

Dose route

Descripción

Dose route

Tipo de datos

text

Alias

UMLS CUI [1,1]: C0013153

UMLS CUI [1,2]: C0679006

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Dosing regime - GSK Study: GW679769 administered alone vs. with dexamethasone - Evaluation of safety, tolerability and pharmacokinetics NCT00291876

1 formularios

StudyEvent: ODM
1. Dosing regime - GSK Study: GW679769 administered alone vs. with dexamethasone - Evaluation of safety, tolerability and pharmacokinetics NCT00291876

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de datos

Alias

drug administration decision

Item Group

Regime selection

C0013153 (UMLS CUI-1)
C0679006 (UMLS CUI-2)

drug administration regime decision

Item

Please select a regime for this subject and this session and press "continue".

integer

C0013153 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])

undefined item

Code List

Please select a regime for this subject and this session and press "continue".

CL Item

O-Single 150mg Oral of GW679769 (1)

CL Item

P-Placebo for IV GW679769 (2)

CL Item

X1-IV GW679769 12mg (3)

CL Item

X2-IV GW679769 12-35mg (4)

CL Item

X3-IV GW679769 35-70mg (5)

CL Item

X4-IV GW679769 70-130mg (6)

Study medication oral

Item Group

Study medication oral

C0013227 (UMLS CUI-1)
C0304229 (UMLS CUI-2)
C1527415 (UMLS CUI-3)

Dosing day

Item

Session day

partialDate

C1883016 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])

Session hour

Item

Session hour

partialDatetime

C1883016 (UMLS CUI [1,1])
C0439227 (UMLS CUI [1,2])

Session minute

Item

Session minute

partialDatetime

C1883016 (UMLS CUI [1,1])
C0439232 (UMLS CUI [1,2])

Start dose date

Item

Start Dose Date

date

C0808070 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

Start dose time

Item

Start Dose Time

time

C1301880 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

Dose amount

Item

Dose amount

integer

C0178602 (UMLS CUI [1,1])
C1264637 (UMLS CUI [1,2])

Dose unit

Item

Dose units

text

C0869039 (UMLS CUI [1])

Dose form

Item

Dose formulation

text

C0013058 (UMLS CUI [1])

Dose route

Item

Dose route

text

C0013153 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])

Study medication IV

Item Group

Study Medication IV

C0013227 (UMLS CUI-1)
C0304229 (UMLS CUI-2)
C1522726 (UMLS CUI-3)

Dosing day

Item

Session day

partialDate

C1883016 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])

Session hour

Item

Session hour

partialDatetime

C1883016 (UMLS CUI [1,1])
C0439227 (UMLS CUI [1,2])

Session minute

Item

Session minute

partialDatetime

C1883016 (UMLS CUI [1,1])
C0439232 (UMLS CUI [1,2])

Start dose date

Item

Start Dose Date

date

C0808070 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

Start dose time

Item

Start Dose Time

time

C1301880 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

End Dose Date

Item

End Dose Date

date

C0806020 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

End Dose Time

Item

End Dose Time

time

C1522314 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])

Start Dose Volume

Item

Start Dose Volume

text

C0449468 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])

End Dose Volume

Item

End Dose Volume

text

C0449468 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0444930 (UMLS CUI [1,3])

Dose amount

Item

Dose amount

integer

C0178602 (UMLS CUI [1,1])
C1264637 (UMLS CUI [1,2])

Dose unit

Item

Dose units

text

C0869039 (UMLS CUI [1])

Dose form

Item

Dose formulation

text

C0013058 (UMLS CUI [1])

Dose route

Item

Dose route

text

C0013153 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])

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