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ID

37869

Beschreibung

Study ID: 111634 Clinical Study ID: 111634 Study Title: A phase III, open, controlled study in South Africa to assess the immunogenicity, safety and reactogenicity of GSK Biologicals’ 10-valent pneumococcal conjugate vaccine administered as a 3-dose (6, 10, 14 weeks) primary immunization course in HIV infected infants, HIV exposed uninfected infants and HIV unexposed uninfected infants followed by a booster vaccination at 9-10 months of age. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00829010 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Pneumococcal vaccine GSK1024850A Trade Name: Tritanrix-HepB/Hib, Rotarix Study Indication: Infections, Streptococcal This phase III trial studies the immunogenicity, safety and reactogenicity of a 10-valent pneumococcal conjugate vaccine in three groups of infants that differ by HIV status: HIV-positive infants, HIV-negative infants who are exposed to the virus (by their HIV-positive mother), and HIV-negative infants who are not exposed. The study consists of Screening at 4-8 weeks of age (only for HIV-positive and HIV-exposed infants without HIV DNA test) and 10 subsequent Visits over a period of 23 months. There are five study cohorts: HIV-positive and HIV-exposed participants receive the vaccine at Visits 1, 2, 3 (i.e. 6, 10 and 14 weeks of life; primary course) and 5 (9-10 months of age; booster), whereas HIV-negative, unexposed infants are randomly assigned to one of three vaccination schedules: the aforementioned schedule consisting of the primary course and the booster, or the 3-dose primary course only without the booster vaccination, or a different primary course consisting of only two vaccinations at Visits 1 and 3 (6 and 14 weeks of age) followed by a booster at Visit 5 (9-10 months). Visit 1 is scheduled at 6-10 weeks of life. The interval between Visits 1 and 2, 2 and 3, as well as 3 and 4 has to be 28-42 days each. Visit 5 then takes place at 9-10 months of age. The interval between Visit 5 and 6 again has to be 28-42 days. Visit 7 is scheduled at 12-13 months of age, Visit 8 at 15-18 months, Visit 9 at 16-19 months, and the final Visit 10 is performed when the subjects are 24-27 months old. This form contains general medical history and physical examination of various organ systems and is to be filled in at Visit 1 for all cohorts.

Stichworte

  1. 28.08.19 28.08.19 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

28. August 2019

DOI

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Creative Commons BY-NC 3.0

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    10-valent pneumococcal vaccine in HIV-positive, HIV-exposed and HIV-negative infants - NCT00829010

    Medical History, Physical Examination

    Administrative data
    Beschreibung

    Administrative data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Subject Identifier
    Beschreibung

    Clinical Trial Subject Unique Identifier

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Cohort
    Beschreibung

    Cohort

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C0599755 (Cohort)
    Date of Visit
    Beschreibung

    Date of Visit

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C1320303 (Date of visit)
    SNOMED
    406543005
    General Medical History / Physical Examination
    Beschreibung

    General Medical History / Physical Examination

    Alias
    UMLS CUI-1
    C0262926 (Medical History)
    SNOMED
    392521001
    LOINC
    LP6817-3
    UMLS CUI-2
    C0031809 (Physical Examination)
    SNOMED
    5880005
    LOINC
    MTHU028014
    Are you aware of any pre-existing conditions or signs and/or symptoms present in the subject prior to the start of the study?
    Beschreibung

    If yes, please give diagnosis in the repeating item group and select appropriate Past/Current box(es)

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0521987 (Pre-existing condition)
    SNOMED
    102478008
    UMLS CUI [2,1]
    C0037088 (Signs and Symptoms)
    SNOMED
    404684003
    LOINC
    LP185402-7
    UMLS CUI [2,2]
    C2347804 (Clinical Trial Period)
    UMLS CUI [2,3]
    C0332152 (Before)
    SNOMED
    236874000
    Diagnosis
    Beschreibung

    Diagnosis

    Alias
    UMLS CUI-1
    C0011900 (Diagnosis)
    SNOMED
    439401001
    LOINC
    LP30831-9
    MedDRA System Organ class
    Beschreibung

    MedDRA System Organ class

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C2347091 (MedDRA System Organ Class)
    Diagnosis
    Beschreibung

    Diagnosis

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0011900 (Diagnosis)
    SNOMED
    439401001
    LOINC
    LP30831-9
    Past medical condition
    Beschreibung

    Selection of both "past" and "current" condition possible.

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0012634 (Disease)
    SNOMED
    64572001
    LOINC
    LP21006-9
    UMLS CUI [1,2]
    C0332119 (Past history of)
    LOINC
    LP100603-2
    Current medical condition
    Beschreibung

    Selection of both "past" and "current" condition possible.

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0521116 (Current (present time))
    SNOMED
    15240007
    UMLS CUI [1,2]
    C0012634 (Disease)
    SNOMED
    64572001
    LOINC
    LP21006-9

    Ähnliche Modelle

    Medical History, Physical Examination

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item
    Cohort
    integer
    C0599755 (UMLS CUI [1])
    Code List
    Cohort
    CL Item
    HIV-pos. (1)
    CL Item
    HIV-neg. exposed (2)
    CL Item
    HIV-neg. unexposed, 3+1 schedule (3)
    CL Item
    HIV-neg. unexposed, 3+0 schedule (4)
    CL Item
    HIV-neg. unexposed, 2+1 schedule (5)
    Date of Visit
    Item
    Date of Visit
    date
    C1320303 (UMLS CUI [1])
    Item Group
    General Medical History / Physical Examination
    C0262926 (UMLS CUI-1)
    C0031809 (UMLS CUI-2)
    Are you aware of any pre-existing conditions or signs and/or symptoms prior to the start of the study?
    Item
    Are you aware of any pre-existing conditions or signs and/or symptoms present in the subject prior to the start of the study?
    boolean
    C0521987 (UMLS CUI [1])
    C0037088 (UMLS CUI [2,1])
    C2347804 (UMLS CUI [2,2])
    C0332152 (UMLS CUI [2,3])
    Item Group
    Diagnosis
    C0011900 (UMLS CUI-1)
    Item
    MedDRA System Organ class
    integer
    C2347091 (UMLS CUI [1])
    Code List
    MedDRA System Organ class
    CL Item
    Eye (10)
    CL Item
    Respiratory, thoracic and mediastinal (5)
    CL Item
    Gastrointestinal (6)
    CL Item
    Musculoskeletal and connective tissue (2)
    CL Item
    Cardiac (3)
    CL Item
    Skin and subcutaneous tissue (1)
    CL Item
    Hepatobiliary (7)
    CL Item
    Renal and urinary (8)
    CL Item
    Endocrine (12)
    CL Item
    Ear and labyrinth (11)
    CL Item
    Vascular (4)
    CL Item
    Nervous system (9)
    CL Item
    Metabolism and nutrition (13)
    CL Item
    Blood and lymphatic system (14)
    CL Item
    Immune system (incl allergies, autoimmune disorders) (15)
    CL Item
    Infections and infestations (16)
    CL Item
    Neoplasms benign, malignant and unspecified (incl cysts, polyps) (17)
    CL Item
    Surgical and medical procedure (18)
    CL Item
    Other (99)
    Diagnosis
    Item
    Diagnosis
    text
    C0011900 (UMLS CUI [1])
    Past medical condition
    Item
    Past medical condition
    boolean
    C0012634 (UMLS CUI [1,1])
    C0332119 (UMLS CUI [1,2])
    Current medical condition
    Item
    Current medical condition
    boolean
    C0521116 (UMLS CUI [1,1])
    C0012634 (UMLS CUI [1,2])

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