ID
32060
Description
Study ID: 103992 Clinical Study ID: 103992 Study Title: Evaluate immunogenicity, reactogenicity & safety of 2 doses of GSK Biologicals’ oral live attenuated HRV vaccine (RIX4414 at 106.5 CCID50) when given concomitantly with OPV versus given alone (HRV vaccine dose given 15 days after the OPV dose) in healthy infants in Bangladesh Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00139334 https://clinicaltrials.gov/ct2/show/NCT00139334 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Rotavirus Vaccine Trade Name: Rotarix Study Indication: Haemophilus influenzae type b; Neisseria Meningitidis This form details Elimination Criteria. They need to be checked at each visit prior to any other procedure, starting form Visit 2. Visit 2 -> Timing: Day 30, Age: 10 weeks +/- 1 week Visit 3 -> Timing: Day 45, Age: 12 weeks +/- 1 week Visit 4 -> Timing: Day 60, Age: 14 weeks +/- 1 week Visit 5 -> Timing: Day 75, Age: 16 weeks +/- 1 week Visit 6 -> Timing: Day 105, Age: 20 weeks +/- 1 week
Link
https://clinicaltrials.gov/ct2/show/NCT00139334
Keywords
Versions (1)
- 10/16/18 10/16/18 - Sarah Riepenhausen
Copyright Holder
GlaxoSmithKline
Uploaded on
October 16, 2018
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
GSK Biologicals' oral HRV vaccine given with OPV in infants NCT00139334
Elimination Criteria during the Study
- StudyEvent: ODM
Description
Elimination Criteria during the Study
Alias
- UMLS CUI-1
- C0680251
Description
previous RV GE
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0035870
- UMLS CUI [1,2]
- C0017160
Description
Diarrhea
Data type
boolean
Alias
- UMLS CUI [1]
- C0011991
Description
investigational or non-registered product (drug or vaccine)
Data type
boolean
Alias
- UMLS CUI [1]
- C0304229
- UMLS CUI [2,1]
- C0042210
- UMLS CUI [2,2]
- C1517586
Description
undefined item
Data type
boolean
Alias
- UMLS CUI [1]
- C0021081
Description
Vaccine administration within 14 days before/after study vaccination nor forseen in study protocol
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C2348563
Description
Immunoglobulins or blood products during study
Data type
boolean
Alias
- UMLS CUI [1]
- C0021027
- UMLS CUI [2]
- C0371802
Description
immunosuppressive or immunodeficient condition, including HIV infection
Data type
boolean
Alias
- UMLS CUI [1]
- C4048329
- UMLS CUI [2]
- C0021051
- UMLS CUI [3]
- C0019693
Similar models
Elimination Criteria during the Study
- StudyEvent: ODM
C0017160 (UMLS CUI [1,2])
C0042210 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
C2348563 (UMLS CUI [1,2])
C0371802 (UMLS CUI [2])
C0021051 (UMLS CUI [2])
C0019693 (UMLS CUI [3])