ID
37971
Descripción
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 the Diary Cards, in which parents/guardians should record local and general symptoms in the first 3 days after the study vaccinations, as well as medication taken since the vaccination. These forms are handed out after the vaccination Visits, i.e. Visits 1, 2, 3 and 8 (all cohorts) and additionally Visit 5 for all cohorts except for the 3+0 schedule without the booster vaccination in HIV-negative subjects. These Diary Cards are transcribed by the investigator, resulting in the Solicited/Unsolicited AE form as well as (part of) the Concomitant Medication form.
Palabras clave
Versiones (2)
- 2/9/19 2/9/19 -
- 3/9/19 3/9/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
3 de septiembre de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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10-valent pneumococcal vaccine in HIV-positive, HIV-exposed and HIV-negative infants - NCT00829010
Diary Cards (Amendment 1)
- StudyEvent: ODM
Descripción
Local Symptoms (at injection sites)
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0205276
- UMLS CUI-3
- C2700396
Descripción
Fill in entire item group once per vaccine The 10Pn-PD-DiT vaccine is administered at Visits 1 (all cohorts), 2 (all cohorts except the 2+1 schedule HIV-neg. cohort), 3 (all cohorts) and 5 (all cohorts except the EPI/3+0 schedule HIV-neg. cohort). The DTPw-HBV/Hib vaccine is administered at Visits 1, 2, 3 and 8 (all cohorts).
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0042196
Descripción
For investigator only: Could you please tick the appropriate box (side / site) for assessment.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0441987
- UMLS CUI [1,2]
- C0013153
- UMLS CUI [1,3]
- C0042210
Descripción
For investigator only: Could you please tick the appropriate box (side / site) for assessment.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1515974
- UMLS CUI [1,2]
- C0013153
- UMLS CUI [1,3]
- C0042210
Descripción
Fill in entire item group once per symptom Record either Size on Days 0-3 for Redness and Swelling or Pain Intensity on Days 0-3 for Pain.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1457887
Descripción
for Redness and Swelling Measure and record the greatest diameter (in mm). The original PDF file contains a printed 0-100 mm scale. The following comment is included in the Diary Cards of the Booster Doses: In case of large swelling reaction at the injected limb, please fill in ALSO the Large Swelling Reaction forms.
Tipo de datos
integer
Unidades de medida
- mm
Alias
- UMLS CUI [1]
- C0456389
Descripción
for Redness and Swelling Measure and record the greatest diameter (in mm). The original PDF file contains a printed 0-100 mm scale. The following comment is included in the Diary Cards of the Booster Doses: In case of large swelling reaction at the injected limb, please fill in ALSO the Large Swelling Reaction forms.
Tipo de datos
integer
Unidades de medida
- mm
Alias
- UMLS CUI [1]
- C0456389
Descripción
for Redness and Swelling Measure and record the greatest diameter (in mm). The original PDF file contains a printed 0-100 mm scale. The following comment is included in the Diary Cards of the Booster Doses: In case of large swelling reaction at the injected limb, please fill in ALSO the Large Swelling Reaction forms.
Tipo de datos
integer
Unidades de medida
- mm
Alias
- UMLS CUI [1]
- C0456389
Descripción
for Redness and Swelling Measure and record the greatest diameter (in mm). The original PDF file contains a printed 0-100 mm scale. The following comment is included in the Diary Cards of the Booster Doses: In case of large swelling reaction at the injected limb, please fill in ALSO the Large Swelling Reaction forms.
Tipo de datos
integer
Unidades de medida
- mm
Alias
- UMLS CUI [1]
- C0456389
Descripción
Intensity: 0 / 1 / 2 / 3
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1320357
Descripción
Intensity: 0 / 1 / 2 / 3
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1320357
Descripción
Intensity: 0 / 1 / 2 / 3
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1320357
Descripción
Intensity: 0 / 1 / 2 / 3
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1320357
Descripción
if yes, give last day of symptoms in next item
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0549178
Descripción
Last Day of Symptoms
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1457887
Descripción
Other local symptoms
Alias
- UMLS CUI-1
- C0205394
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
Descripción
Local symptom description
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0205276
- UMLS CUI [1,3]
- C0678257
Descripción
Symptom Intensity
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
Symptom start date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Descripción
If no, record end date
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0549178
Descripción
if not continuing
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Descripción
General Symptoms
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C0042196
Descripción
Fill in entire item group once per symptom Diarrhoea and Vomiting are only applicable if HRV has been administered (Visit 2 and 3)
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1457887
Descripción
Please record the temperature every day in the evening. Should additional temperature measurements be performed at other times of the day, the highest temperature is to be recorded.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0489453
Descripción
Body Temperature on Day 0
Tipo de datos
float
Unidades de medida
- C
Alias
- UMLS CUI [1]
- C0005903
Descripción
Body Temperature on Day 1
Tipo de datos
float
Unidades de medida
- C
Alias
- UMLS CUI [1]
- C0005903
Descripción
Body Temperature on Day 2
Tipo de datos
float
Unidades de medida
- C
Alias
- UMLS CUI [1]
- C0005903
Descripción
Body Temperature on Day 3
Tipo de datos
float
Unidades de medida
- C
Alias
- UMLS CUI [1]
- C0005903
Descripción
For Irritability/Fussiness: 0 = Behavior as usual 1 = Crying more than usual / no effect on normal activity 2 = Crying more than usual / interferes with normal activity 3 = Crying that cannot be comforted / prevents normal activity For Drowsiness: 0 = Behavior as usual 1 = Drowsiness easily tolerated 2 = Drowsiness that interferes with normal activity 3 = Drowsiness that prevents normal activity For Loss of appetite: 0 = Appetite as usual 1 = Eating less than usual / no effect on normal activity 2 = Eating less than usual / interferes with normal activity 3 = Not eating at all
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
For Irritability/Fussiness: 0 = Behavior as usual 1 = Crying more than usual / no effect on normal activity 2 = Crying more than usual / interferes with normal activity 3 = Crying that cannot be comforted / prevents normal activity For Drowsiness: 0 = Behavior as usual 1 = Drowsiness easily tolerated 2 = Drowsiness that interferes with normal activity 3 = Drowsiness that prevents normal activity For Loss of appetite: 0 = Appetite as usual 1 = Eating less than usual / no effect on normal activity 2 = Eating less than usual / interferes with normal activity 3 = Not eating at all
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
For Irritability/Fussiness: 0 = Behavior as usual 1 = Crying more than usual / no effect on normal activity 2 = Crying more than usual / interferes with normal activity 3 = Crying that cannot be comforted / prevents normal activity For Drowsiness: 0 = Behavior as usual 1 = Drowsiness easily tolerated 2 = Drowsiness that interferes with normal activity 3 = Drowsiness that prevents normal activity For Loss of appetite: 0 = Appetite as usual 1 = Eating less than usual / no effect on normal activity 2 = Eating less than usual / interferes with normal activity 3 = Not eating at all
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
For Irritability/Fussiness: 0 = Behavior as usual 1 = Crying more than usual / no effect on normal activity 2 = Crying more than usual / interferes with normal activity 3 = Crying that cannot be comforted / prevents normal activity For Drowsiness: 0 = Behavior as usual 1 = Drowsiness easily tolerated 2 = Drowsiness that interferes with normal activity 3 = Drowsiness that prevents normal activity For Loss of appetite: 0 = Appetite as usual 1 = Eating less than usual / no effect on normal activity 2 = Eating less than usual / interferes with normal activity 3 = Not eating at all
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
For Diarrhoea, record the number of looser than normal stools per day. For Vomiting, record the number of vomiting episodes per day.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0750480
- UMLS CUI [1,2]
- C0332189
- UMLS CUI [1,3]
- C0439505
Descripción
For Diarrhoea, record the number of looser than normal stools per day. For Vomiting, record the number of vomiting episodes per day.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0750480
- UMLS CUI [1,2]
- C0332189
- UMLS CUI [1,3]
- C0439505
Descripción
For Diarrhoea, record the number of looser than normal stools per day. For Vomiting, record the number of vomiting episodes per day.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0750480
- UMLS CUI [1,2]
- C0332189
- UMLS CUI [1,3]
- C0439505
Descripción
For Diarrhoea, record the number of looser than normal stools per day. For Vomiting, record the number of vomiting episodes per day.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0750480
- UMLS CUI [1,2]
- C0332189
- UMLS CUI [1,3]
- C0439505
Descripción
if yes, give last day of symptoms in next item
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0549178
Descripción
Last Day of Symptoms
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1457887
Descripción
Other General Symptoms
Alias
- UMLS CUI-1
- C0029625
Descripción
General symptom description
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0678257
Descripción
Symptom Intensity
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0518690
Descripción
Symptom start date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Descripción
If no, record end date
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0549178
Descripción
if not continuing
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Descripción
Medication
Alias
- UMLS CUI-1
- C2347852
Descripción
Concomitant Medication name
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Descripción
Concomitant Medication Reason
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C2347852
Descripción
Concomitant Medication Daily Dose
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826638
Descripción
Concomitant Medication start date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2826734
Descripción
if not continuing
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2826744
Descripción
If no, specify end date
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2826666
Similar models
Diary Cards (Amendment 1)
- StudyEvent: ODM
C0332152 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,3])
C0042196 (UMLS CUI [1,2])
C3890583 (UMLS CUI [1,2])
C1548100 (UMLS CUI [1,3])
C1515258 (UMLS CUI [1,2])
C0205276 (UMLS CUI-2)
C2700396 (UMLS CUI-3)
C0013153 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,3])
C0013153 (UMLS CUI [1,2])
C0042210 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0205276 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0332189 (UMLS CUI [1,2])
C0439505 (UMLS CUI [1,3])
C0332189 (UMLS CUI [1,2])
C0439505 (UMLS CUI [1,3])
C0332189 (UMLS CUI [1,2])
C0439505 (UMLS CUI [1,3])
C0332189 (UMLS CUI [1,2])
C0439505 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0678257 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])