ID

37869

Descrizione

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.

Keywords

  1. 28/08/19 28/08/19 -
Titolare del copyright

GlaxoSmithKline

Caricato su

28 agosto 2019

DOI

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Licenza

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
Descrizione

Administrative data

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

Clinical Trial Subject Unique Identifier

Tipo di dati

integer

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

Cohort

Tipo di dati

integer

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

Date of Visit

Tipo di dati

date

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

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?
Descrizione

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

Tipo di dati

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
Descrizione

Diagnosis

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

MedDRA System Organ class

Tipo di dati

integer

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

Diagnosis

Tipo di dati

text

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

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

Tipo di dati

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
Descrizione

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

Tipo di dati

boolean

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

Similar models

Medical History, Physical Examination

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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