ID
29477
Description
A multicenter study of the immunogenicity & safety of 2 doses of GSK Biologicals’oral live attenuated human rotavirus vaccine (RIX4414) as primary dosing of healthy infants in India aged approximately 8 wks at the time of the first dose
Mots-clés
Versions (2)
- 31/03/2018 31/03/2018 -
- 04/04/2018 04/04/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
31 mars 2018
DOI
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Licence
Creative Commons BY-NC 3.0
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Rotavirus Vaccine RIX4414 Study 103792
Study Conclusion
- StudyEvent: ODM
Description
Occurrence of serious adverse event
Alias
- UMLS CUI-1
- C1519255
Description
Serious adverse event
Type de données
boolean
Alias
- UMLS CUI [1]
- C1519255
Description
Only answer if you chose 'yes'a s previous answer.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449788
Description
Status of treatment blind
Description
If yes, complete Non-Serious Adverse Events, Serious Adverse Event and/or Investigational Product forms as appropriate
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0749659
- UMLS CUI [1,2]
- C2347038
Description
Date blind broken
Type de données
date
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
Description
Reason blind broken
Type de données
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
Description
Reason blind broken - other
Type de données
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
Description
Elimination criteria
Alias
- UMLS CUI-1
- C0680251
Description
Elimination criteria
Type de données
boolean
Alias
- UMLS CUI [1]
- C0680251
Description
specify elimination criteria
Type de données
text
Alias
- UMLS CUI [1,1]
- C0680251
- UMLS CUI [1,2]
- C1521902
Description
Study Withdrawal
Alias
- UMLS CUI-1
- C2348568
Description
withdrawn
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0008976
Description
If Yes, please specify
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0008976
Description
If Serious adverse event, please specify
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0237753
Description
If Non-serious adverse event, please specify
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0237753
Description
Protocol violation
Type de données
text
Alias
- UMLS CUI [1]
- C1709750
Description
If Other, please specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0008976
Description
reason for withdrawal
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0008976
Description
Date of last contact
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1705415
Description
subject condition
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1142435
- UMLS CUI [1,2]
- C0681850
Description
Investigators signature
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
Investigators signature Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2346576
Similar models
Study Conclusion
- StudyEvent: ODM
C0449788 (UMLS CUI [1,2])
C2347038 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C1705415 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,2])
C2346576 (UMLS CUI [1,2])