ID

41672

Beskrivning

Study ID: 105874 Clinical Study ID: 105874 Study Title: Bridging Safety & Immunogenicity Study of GSK Biologicals' Candidate Malaria Vaccine RTS,S/AS01E (0.5 mL Dose) to RTS,S/AS02D (0.5 mL Dose) Administered IM According to a 0, 1, 2-Month Schedule in Gabonese Children Aged 18 Months to 4 Years Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00307021 https://clinicaltrials.gov/ct2/show/NCT00307021 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK Biologicals' candidate Plasmodium falciparum malaria vaccine 257049 Trade Name: N/A Study Indication: Malaria This study has a total of 7 visits. Visit 1 = Screening, Visits 2-6 are during the double-blind phase (Month 0-3) and Visit 7 is during the single-blind phase (Month 4-14). This form (Contraindications to subsequent vaccination) should be filled out whenever a vaccination is due. Indications for deferral of vaccination: The following AEs constitute contraindications to administration of RTS,S/AS02D or RTS,S/AS01E at that point in time; if any one of these AEs occur at the time scheduled for vaccination, the subject may be vaccinated at a later date, within the time window specified in the protocol, or withdrawn at the discretion of the investigator. Absolute contraindications to further vaccination: The following AEs constitute absolute contraindications to further administration of RTS,S/AS02D or RTS,S/AS01E; if any of these AEs occur during the study, the subject must not receive additional doses of vaccine, but may continue other study procedures at the discretion of the investigator.

Länk

https://clinicaltrials.gov/ct2/show/NCT00307021

Nyckelord

  1. 2020-12-09 2020-12-09 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

9 december 2020

DOI

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Licens

Creative Commons BY-NC 4.0

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Safety & Immunogenicity of two GSK Biologicals' Candidate Malaria Vaccines in young children, NCT00307021

Contraindications to subsequent vaccination

Administrative Data
Beskrivning

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject number
Beskrivning

Subject number

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Date of visit/assessment
Beskrivning

Date of visit/assessment

Datatyp

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
Indications for deferral of vaccination
Beskrivning

Indications for deferral of vaccination

Alias
UMLS CUI-1
C0205421
UMLS CUI-2
C0042196
UMLS CUI-3
C3146298
[A] Acute disease at the time of administration of investigational product (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhea or mild upper respiratory infection without fever, i.e. axillary temperature < 37.5°C.
Beskrivning

Acute disease at the time of administration of investigational product

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0001314
UMLS CUI [1,2]
C0150312
UMLS CUI [1,3]
C2368628
[B] Axillary temperature of >= 37.5°C.
Beskrivning

Axillary temperature

Datatyp

boolean

Alias
UMLS CUI [1]
C1531924
Absolute contraindications to further vaccination
Beskrivning

Absolute contraindications to further vaccination

Alias
UMLS CUI-1
C0522473
UMLS CUI-2
C0042196
[C] Acute allergic reaction (significant IgE-mediated events) or anaphylaxis following the administration of vaccine investigational product.
Beskrivning

Acute allergic reaction or anaphylaxis following administration of vaccine

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0042196
UMLS CUI [1,2]
C0020517
UMLS CUI [2,1]
C0002792
UMLS CUI [2,2]
C0042196
[D] Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
Beskrivning

Immunosuppressive or immunodeficient condition, including HIV

Datatyp

boolean

Alias
UMLS CUI [1]
C4048329
UMLS CUI [2]
C0021051
UMLS CUI [3]
C0019693
[E] Failure to thrive.
Beskrivning

Failure to thrive

Datatyp

boolean

Alias
UMLS CUI [1]
C0015544

Similar models

Contraindications to subsequent vaccination

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Date of visit/assessment
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
Item Group
Indications for deferral of vaccination
C0205421 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
C3146298 (UMLS CUI-3)
Acute disease at the time of administration of investigational product
Item
[A] Acute disease at the time of administration of investigational product (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhea or mild upper respiratory infection without fever, i.e. axillary temperature < 37.5°C.
boolean
C0001314 (UMLS CUI [1,1])
C0150312 (UMLS CUI [1,2])
C2368628 (UMLS CUI [1,3])
Axillary temperature
Item
[B] Axillary temperature of >= 37.5°C.
boolean
C1531924 (UMLS CUI [1])
Item Group
Absolute contraindications to further vaccination
C0522473 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
Acute allergic reaction or anaphylaxis following administration of vaccine
Item
[C] Acute allergic reaction (significant IgE-mediated events) or anaphylaxis following the administration of vaccine investigational product.
boolean
C0042196 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0002792 (UMLS CUI [2,1])
C0042196 (UMLS CUI [2,2])
Immunosuppressive or immunodeficient condition, including HIV
Item
[D] Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
boolean
C4048329 (UMLS CUI [1])
C0021051 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
Failure to thrive
Item
[E] Failure to thrive.
boolean
C0015544 (UMLS CUI [1])

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