ID
32299
Description
Study ID: 109563 Clinical Study ID: 109563 Study Title: COMPAS:A phase III study to demonstrate efficacy of GSK Biologicals' 10-valent pneumococcal vaccine (GSK1024850A) against Community Acquired Pneumonia and Acute Otitis Media Patient Level Data: Study Listed on https://clinicaltrials.gov/ct2/show/NCT00466947 https://clinicalstudydatarequest.com/Posting.aspx?ID=2809 Clinicaltrials.gov Identifier: NCT00466947 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Pneumococcal Polysaccharide Conjugate Vaccine (Adsorbed) Trade Name: BIO 10PN-PD-DIT; Synflorix Study Indication: Infections, Streptococcal The Study consists of three workbooks. Workbook 1: Argentina, all subjects + immuno & reacto subset Workbook 2: Panama, all subjects + immuno & reacto subset + carriage subset + additional immuno subset Workbook 3: Colombia, all subjects The protocol number for all workbooks: 109563 (10Pn-PD-DiT-028) There are ten visits in workbook 1 and 2, eight for workbook 3 (there are no visits 4 and 7): Visit 1: month 0, dose 1, 6-16 weeks of age Visit 2: month 2, dose 2, +/- 4 months of age, 49-83 days after visit 1 Visit 3: month 4, dose 3, +/- 6 months of age, 49-83 days after visit 2 Visit 4: month 5, +/- 7 months of age, 28-42 days after visit 3. Only for immuno & reacto subset + carriage subset. Visit 5: month 10-13, 12-15 months of age Visit 6: month 13-16, booster dose, 15-18 months of age, ≥ 28 days after visit 5 Visit 7: month 14-17, 16-19 months of age, 28-42 days after visit 6. Only for immuno & reacto subset, additional immuno subset + carriage subset. Visit 8: month 16-19, 18-21 months of age, ≥ 28 days after visit 6 Visit 9: month 22-25, 24-27 months of age Visit 10: Contact This document contains the protocol required concomitant vaccination. It has to be filled in for Visit 5 and 8. In Visit 8 only HAV has to be administered. It's for all workbooks. The document also contains the convulsion episode. It's for all workbooks and has to be filled in only in Visit 8.
Lien
https://clinicaltrials.gov/ct2/show/NCT00466947
Mots-clés
Versions (3)
- 23/10/2018 23/10/2018 -
- 26/10/2018 26/10/2018 -
- 26/10/2018 26/10/2018 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
26 octobre 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Vaccination against pneumonia and otitis media, NCT00466947
Protocol required concomitant vaccination, convulsion episode
- StudyEvent: ODM
Description
PROTOCOL REQUIRED CONCOMITANT VACCINATION
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C0042196
- UMLS CUI-3
- C1708545
Description
If Yes is ticked, the applicable vaccine is not to be reported again in the Concomitant Vaccination section at the end of the CRF. Any other vaccines administered during the study period are to be recorded in the Concomitant Vaccination section at the end of the CRF. Reminder: Any vaccine should be administered at least 30 days before the date of study vaccine administration.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C1708545
- UMLS CUI [1,4]
- C2368628
Description
In visit 8 only HAV vaccine
Type de données
integer
Alias
- UMLS CUI [1]
- C0042210
Description
Vaccine administration, Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2368628
Description
CONVULSION EPISODE
Alias
- UMLS CUI-1
- C0332189
- UMLS CUI-2
- C4048158
Description
If yes please complete the CONVULSION EPISODE section
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332189
- UMLS CUI [1,2]
- C4048158
- UMLS CUI [1,3]
- C0332282
- UMLS CUI [1,4]
- C0042196
- UMLS CUI [1,5]
- C3259236
Similar models
Protocol required concomitant vaccination, convulsion episode
- StudyEvent: ODM
C0042196 (UMLS CUI-2)
C1708545 (UMLS CUI-3)
C0042196 (UMLS CUI [1,2])
C1708545 (UMLS CUI [1,3])
C2368628 (UMLS CUI [1,4])
C2368628 (UMLS CUI [1,2])
C4048158 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,3])
C0042196 (UMLS CUI [1,4])
C3259236 (UMLS CUI [1,5])