ID

34359

Beskrivning

Study ID: 101682 Clinical Study ID: B2E101682 Study Title: A randomised, double-blind, placebo-controlled, parallel group study to examine the safety, tolerability, and pharmacokinetics of repeat inhaled doses of GSK159797 in healthy subjects. Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: milveterol Study Indication: Pulmonary Disease, Chronic Obstructive. This form contains information about concomitant medications and should be completed only in case of concomitant medication.

Nyckelord

Versioner (2)
  1. 2019-01-16 2019-01-16 -
  2. 2019-01-16 2019-01-16 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0
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Safety, tolerability and pharmacokinetics of repeat inhaled doses of milveterol in healthy subjects (Study ID: 101682)

Engelsk

Concomitant Medications

1 Formulär  
Concomitant Medications
Beskrivning

Concomitant Medications

Alias
UMLS CUI-1
C1704627
Were any concomitant medications taken by the subject during the study?
Beskrivning

concomitant medications during study

Datatyp

boolean

Alias
UMLS CUI [1]
C1707479
Drug (Trade name preferred)
Beskrivning

If medication is given to treat an adverse event, then the ADVERSE EVENT must be recorded on the NON-SERIOUS ADVERSE EVENT or SERIOUS ADVERSE EVENT page(s).

Datatyp

text

Alias
UMLS CUI [1]
C2347852
Dose
Beskrivning

Dose

Datatyp

float

Alias
UMLS CUI [1]
C2826638
Unit
Beskrivning

Unit

Datatyp

text

Alias
UMLS CUI [1]
C2826646
Frequency
Beskrivning

Frequency

Datatyp

text

Alias
UMLS CUI [1]
C2826654
Route
Beskrivning

Route

Datatyp

text

Alias
UMLS CUI [1]
C2826730
Date started
Beskrivning

Start Date

Datatyp

date

Måttenheter
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C2826734
dd.mm.yyyy
Started pre-study
Beskrivning

Started pre-study

Datatyp

boolean

Alias
UMLS CUI [1]
C2981448
Start time
Beskrivning

Start time

Datatyp

time

Måttenheter
  • hh:mm
Alias
UMLS CUI [1]
C2826740
hh:mm
Date stopped
Beskrivning

Stop Date

Datatyp

date

Måttenheter
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C2826744
dd.mm.yyyy
Medication continued post-study
Beskrivning

Ongoing Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
Stop time
Beskrivning

Stop time

Datatyp

time

Måttenheter
  • hh:mm
Alias
UMLS CUI [1]
C2826659
hh:mm
Conditions treated/indication
Beskrivning

Reason for Medication

Datatyp

text

Alias
UMLS CUI [1]
C2826696
Was drug administered for an adverse event?
Beskrivning

drug administered for an adverse event

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2826696
UMLS CUI [1,2]
C0877248
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Similar models

Concomitant Medications

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Concomitant Medications
C1704627 (UMLS CUI-1)
concomitant medications during study
Item
Were any concomitant medications taken by the subject during the study?
boolean
C1707479 (UMLS CUI [1])
Drug Name
Item
Drug (Trade name preferred)
text
C2347852 (UMLS CUI [1])
Dose
Item
Dose
float
C2826638 (UMLS CUI [1])
Unit
Item
Unit
text
C2826646 (UMLS CUI [1])
Frequency
Item
Frequency
text
C2826654 (UMLS CUI [1])
Route
Item
Route
text
C2826730 (UMLS CUI [1])
Start Date
Item
Date started
date
C2826734 (UMLS CUI [1])
Started pre-study
Item
Started pre-study
boolean
C2981448 (UMLS CUI [1])
Start time
Item
Start time
time
C2826740 (UMLS CUI [1])
Stop Date
Item
Date stopped
date
C2826744 (UMLS CUI [1])
Ongoing Medication
Item
Medication continued post-study
boolean
C2826666 (UMLS CUI [1])
Stop time
Item
Stop time
time
C2826659 (UMLS CUI [1])
Reason for Medication
Item
Conditions treated/indication
text
C2826696 (UMLS CUI [1])
drug administered for an adverse event
Item
Was drug administered for an adverse event?
boolean
C2826696 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Tillbaka till toppen 

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