ID

23895

Beschrijving

Study part: Check for Study Continuation Visit 2. A phase 2 study to assess safety, reactogenicity and immunogenicity of a booster dose of an investigational vaccination regimen and GSK Biologicals Hib-MenC vaccine (co-administered with Infanrix penta) compared to a booster dose of Menjugate (co-administered with Infanrix hexa).Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Study ID: 100381, Clinical Study ID: 100381

Trefwoorden

Versies (1)
  1. 16-07-17 16-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

16 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Check for Study Continuation Visit 2 Hib-MenCY-TT-004 BST 003 Neisseria Meningitidis-Haemophilus influenzae type b Vaccine 100381

Engels

Check for Study Continuation Visit 2

1 Formulieren  
CHECK FOR STUDY CONTINUATION
Beschrijving

CHECK FOR STUDY CONTINUATION

Alias
UMLS CUI-1
C0805733
UMLS CUI-2
C0008976
Subject number
Beschrijving

Subject number

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Did the subject come at visit 2 ?
Beschrijving

visit

Datatype

boolean

Alias
UMLS CUI [1]
C0545082
If no, (SAE) Serious adverse event (complete the Serious Adverse Event form)?
Beschrijving

SAE

Datatype

boolean

Alias
UMLS CUI [1]
C1519255
Please specify SAE N° :
Beschrijving

SAE

Datatype

text

Alias
UMLS CUI [1]
C1519255
If no, (AEX) Non-Serious adverse event (complete the Non-serious Adverse Event page)?
Beschrijving

Non-Serious adverse event

Datatype

boolean

Alias
UMLS CUI [1]
C1518404
Please specify AE N° (Unsol.) or code (Solicited) :
Beschrijving

Non-Serious adverse event

Datatype

text

Alias
UMLS CUI [1]
C1518404
(OTH) Other, please specify :
Beschrijving

(e.g. : consent withdrawal, Protocol violation, …)

Datatype

text

Alias
UMLS CUI [1]
C0205394
Investigator's decision
Beschrijving

Investigator desicion study discontinuation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C2826233
Parents/Guardian’s decision
Beschrijving

Parents desicion study discontinuation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030551
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C2826233
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Similar models

Check for Study Continuation Visit 2

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
CHECK FOR STUDY CONTINUATION
C0805733 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
visit
Item
Did the subject come at visit 2 ?
boolean
C0545082 (UMLS CUI [1])
SAE
Item
If no, (SAE) Serious adverse event (complete the Serious Adverse Event form)?
boolean
C1519255 (UMLS CUI [1])
SAE
Item
Please specify SAE N° :
text
C1519255 (UMLS CUI [1])
Non-Serious adverse event
Item
If no, (AEX) Non-Serious adverse event (complete the Non-serious Adverse Event page)?
boolean
C1518404 (UMLS CUI [1])
Non-Serious adverse event
Item
Please specify AE N° (Unsol.) or code (Solicited) :
text
C1518404 (UMLS CUI [1])
other
Item
(OTH) Other, please specify :
text
C0205394 (UMLS CUI [1])
Investigator desicion study discontinuation
Item
Investigator's decision
boolean
C0008961 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C2826233 (UMLS CUI [1,3])
Parents desicion study discontinuation
Item
Parents/Guardian’s decision
boolean
C0030551 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C2826233 (UMLS CUI [1,3])
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