ID

34362

Beschreibung

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.

Stichworte

Versionen (2)
  1. 16.01.19 16.01.19 -
  2. 16.01.19 16.01.19 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

16. Januar 2019

DOI

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Lizenz

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)

Englisch

Concomitant Medications

1 Formulare  
Administrative data
Beschreibung

Administrative data

Alias
UMLS CUI-1
C1320722
Subject number
Beschreibung

Subject number

Datentyp

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Beschreibung

Concomitant Medications

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

concomitant medications during study

Datentyp

boolean

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

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).

Datentyp

text

Alias
UMLS CUI [1]
C2347852
Dose
Beschreibung

Dose

Datentyp

float

Alias
UMLS CUI [1]
C2826638
Unit
Beschreibung

Unit

Datentyp

text

Alias
UMLS CUI [1]
C2826646
Frequency
Beschreibung

Frequency

Datentyp

text

Alias
UMLS CUI [1]
C2826654
Route
Beschreibung

Route

Datentyp

text

Alias
UMLS CUI [1]
C2826730
Date started
Beschreibung

Start Date

Datentyp

date

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

Started pre-study

Datentyp

boolean

Alias
UMLS CUI [1]
C2981448
Start time
Beschreibung

Start time

Datentyp

time

Maßeinheiten
  • hh:mm
Alias
UMLS CUI [1]
C2826740
hh:mm
Date stopped
Beschreibung

Stop Date

Datentyp

date

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

Ongoing Medication

Datentyp

boolean

Alias
UMLS CUI [1]
C2826666
Stop time
Beschreibung

Stop time

Datentyp

time

Maßeinheiten
  • hh:mm
Alias
UMLS CUI [1]
C2826659
hh:mm
Conditions treated/indication
Beschreibung

Reason for Medication

Datentyp

text

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

drug administered for an adverse event

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2826696
UMLS CUI [1,2]
C0877248
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Ähnliche Modelle

Concomitant Medications

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
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])
Zum Seitenanfang zurückkehren 

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