ID

32941

Beschrijving

Study ID: 106181 Clinical Study ID: B2C106181 Study Title: An open-label, single-arm study to determine the excretion balance and metabolic disposition of [14C]GW642444 administered as a single dose of an oral solution to healthy male volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01286831 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: vilanterol Trade Name: Study Indication: Pulmonary Disease, Chronic Obstructive

Trefwoorden

Versies (3)
  1. 09-10-18 09-10-18 -
  2. 10-10-18 10-10-18 -
  3. 21-11-18 21-11-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

21 november 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Extension balance and metabolic disposition of vilanterol as a single oral dose. 106181

Engels

Study conclusion

1 Formulieren  
  1. StudyEvent: ODM
    1. Study conclusion
Study conclusion
Beschrijving

Study conclusion

Date of last contact
Beschrijving

Date last contact

Datatype

date

Alias
UMLS CUI [1]
C0805839
Was the subject withdrawn from the study?
Beschrijving

Patient withdrawn from trial

Datatype

boolean

Alias
UMLS CUI [1]
C0422727
if "Yes" choose one primary reason for withdrawal:
Beschrijving

Patient withdrawn from trial, Indication

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C3146298
Date of decision to withdraw
Beschrijving

Patient withdrawn from trial, Decision, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C0011008
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Similar models

Study conclusion

1 Formulieren
  1. StudyEvent: ODM
    1. Study conclusion
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Study conclusion
Date last contact
Item
Date of last contact
date
C0805839 (UMLS CUI [1])
Patient withdrawn from trial
Item
Was the subject withdrawn from the study?
boolean
C0422727 (UMLS CUI [1])
Item
if "Yes" choose one primary reason for withdrawal:
text
C0422727 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
if "Yes" choose one primary reason for withdrawal:
Code List
if "Yes" choose one primary reason for withdrawal:
CL Item
[1] Adverse event -> Record retails on the Non-Serious Adverse Events or Serious Adverse Events pages as appropriate (1)
CL Item
[3] Protocol deviation (2)
CL Item
[5] Study closed/terminated (3)
CL Item
[6] Lost to follow-up (4)
CL Item
[8] Withdrew consent (Only choose when none of the primary reasons are appropriate) (5)
Patient withdrawn from trial, Decision, Date in time
Item
Date of decision to withdraw
date
C0422727 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Terug naar het begin van de pagina 

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