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ID

33322

Beschreibung

Study ID: 104065 Clinical Study ID: 104065 Study Title: Immune memory of GSK's DTPw-HBV/Hib vaccine by giving Plain PRP polysaccharide at 10 mths. Immuno & reacto of a booster dose of DTPw-HBV/Hib or DTPw-HBV or DTPw-HBV+Hib at 15-18 mths in infants previously primed with DTPw-HBV/Hib Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00169442  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completet Generic Name: Combined Diphtheria, Tetanus, Whole Cell Pertussis, Hepatitis B, Haemophilus influenzae Type b Vaccine (KFT) Trade Name: Zilbrix/Hib Study Indication: Diphtheria; Haemophilus influenzae type b; Hepatitis B; Tetanus; Whole Cell Pertussis

Stichworte

  1. 05.12.18 05.12.18 -
Rechteinhaber

GSK group of companies

Hochgeladen am

5. Dezember 2018

DOI

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Creative Commons BY-NC 3.0

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    Immune memory of Combined Diphtheria, Tetanus, Whole Cell Pertussis, Hepatitis B, Haemophilus influenzae Type b Vaccine at infants (15 to 18 mths) - 104065

    Visit 1: Vaccine Administration

    Administrative data
    Beschreibung

    Administrative data

    Subject Number
    Beschreibung

    Subject Number

    Datentyp

    integer

    Protocol number
    Beschreibung

    Protocol number

    Datentyp

    integer

    Vaccine Administration
    Beschreibung

    Vaccine Administration

    Date
    Beschreibung

    Date

    Datentyp

    date

    Pre-Vaccination temperature
    Beschreibung

    Pre-Vaccination temperature

    Datentyp

    float

    Maßeinheiten
    • °C
    °C
    Route
    Beschreibung

    Route

    Datentyp

    text

    Vaccine Administration
    Beschreibung

    Vaccine Administration

    tick only one box:
    Beschreibung

    tick only one box:

    Datentyp

    text

    Replacement vial number
    Beschreibung

    if applies

    Datentyp

    integer

    Wrong vial number
    Beschreibung

    If applies

    Datentyp

    integer

    Administration side/site/route
    Beschreibung

    Administration side/site/route

    Side and site
    Beschreibung

    Side and site

    Datentyp

    text

    Route
    Beschreibung

    Route

    Datentyp

    text

    Administration according to protocol
    Beschreibung

    Administration according to protocol

    Has the study vaccine been administered according to the Protocol?
    Beschreibung

    Has the study vaccine been administered according to the Protocol?

    Datentyp

    text

    Side
    Beschreibung

    Side

    Datentyp

    text

    Site
    Beschreibung

    Site

    Datentyp

    text

    Route
    Beschreibung

    Route

    Datentyp

    text

    Non-administration
    Beschreibung

    Non-administration

    Why was vaccine not administered?
    Beschreibung

    please tick ONE most appropriate category for non admonistration

    Datentyp

    text

    If Other, please specify
    Beschreibung

    e.g., consent withdrawal, protocol violation

    Datentyp

    text

    If SAE, please specify SAE number
    Beschreibung

    If SAE, please specify SAE number

    Datentyp

    integer

    If Non-SAE, please specify unsolicited AE number
    Beschreibung

    If Non-SAE, please specify unsolicited AE number

    Datentyp

    integer

    Please tick who took the decision
    Beschreibung

    Please tick who took the decision

    Datentyp

    text

    Immediate Post-Vaccination Observation
    Beschreibung

    Immediate Post-Vaccination Observation

    If any AE occurred during the immediate post-vaccination time (30 min), please fill in the Solicited Adverse Events section, the Non-SAE section or a SAE section.
    Beschreibung

    If any AE occurred during the immediate post-vaccination time (30 min), please fill in the Solicited Adverse Events section, the Non-SAE section or a SAE section.

    Datentyp

    text

    If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick "Prophylactic" box.
    Beschreibung

    If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick "Prophylactic" box.

    Datentyp

    text

    Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.
    Beschreibung

    Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.

    Datentyp

    text

    Ähnliche Modelle

    Visit 1: Vaccine Administration

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative data
    Subject Number
    Item
    Subject Number
    integer
    Protocol number
    Item
    Protocol number
    integer
    Item Group
    Vaccine Administration
    Date
    Item
    Date
    date
    Pre-Vaccination temperature
    Item
    Pre-Vaccination temperature
    float
    Item
    Route
    text
    Code List
    Route
    CL Item
    Axillary (1)
    CL Item
    Oral (2)
    CL Item
    Tympanic (oral conversion) (3)
    CL Item
    Tympanic (rectal conversion) (4)
    CL Item
    Rectal (5)
    Item Group
    Vaccine Administration
    Item
    tick only one box:
    text
    Code List
    tick only one box:
    CL Item
    Plain PRP Vaccine (1)
    CL Item
    Replacement vial (2)
    CL Item
    Wrong vial number (3)
    CL Item
    Not administered (4)
    Replacement vial number
    Item
    Replacement vial number
    integer
    Wrong vial number
    Item
    Wrong vial number
    integer
    Item Group
    Administration side/site/route
    Item
    Side and site
    text
    Code List
    Side and site
    CL Item
    Upper right thigh (1)
    Item
    Route
    text
    Code List
    Route
    CL Item
    IM (1)
    Item Group
    Administration according to protocol
    Item
    Has the study vaccine been administered according to the Protocol?
    text
    Code List
    Has the study vaccine been administered according to the Protocol?
    CL Item
    Yes (1)
    CL Item
    No -> please tick all below items that apply (2)
    Item
    Side
    text
    Code List
    Side
    CL Item
    Upper left (1)
    CL Item
    Lower left (2)
    CL Item
    Upper right (3)
    CL Item
    Lower right (4)
    Item
    Site
    text
    Code List
    Site
    CL Item
    Deltoid (1)
    CL Item
    Thigh (2)
    CL Item
    Buttock (3)
    Item
    Route
    text
    Code List
    Route
    CL Item
    I.M. (1)
    CL Item
    S.C. (2)
    Item Group
    Non-administration
    Item
    Why was vaccine not administered?
    text
    Code List
    Why was vaccine not administered?
    CL Item
    Serious Adverse Event (1)
    CL Item
    Non-Serious Adverse Event  (2)
    CL Item
    Other (3)
    If Other, please specify
    Item
    If Other, please specify
    text
    If SAE, please specify SAE number
    Item
    If SAE, please specify SAE number
    integer
    If Non-SAE, please specify unsolicited AE number
    Item
    If Non-SAE, please specify unsolicited AE number
    integer
    Item
    Please tick who took the decision
    text
    Code List
    Please tick who took the decision
    CL Item
    Investigator (1)
    CL Item
    Parents/Guardians (2)
    Item Group
    Immediate Post-Vaccination Observation
    If any AE occurred during the immediate post-vaccination time (30 min), please fill in the Solicited Adverse Events section, the Non-SAE section or a SAE section.
    Item
    If any AE occurred during the immediate post-vaccination time (30 min), please fill in the Solicited Adverse Events section, the Non-SAE section or a SAE section.
    text
    If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick "Prophylactic" box.
    Item
    If any prophylactic medication has been administered in anticipation of study vaccine reaction, please complete the Medication section and tick "Prophylactic" box.
    text
    Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.
    Item
    Any other vaccines administered during the study period must be recorded in the Concomitant Vaccination section.
    text

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