ID
35813
Descripción
Study ID: 102370 (primary study) Clinical Study ID: 102370 Study Title: A multicentre when given according to the 2-4-6 month schedule to healthy infants with booster dose at 12 to 15 months Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00134719 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Haemophilus influenzae Type b, Meningococcal C and Y-Tetanus Toxoid Conjugate Vaccine Trade Name: BIO HIB-MENCY-TT; MenHibrix Study Indication: Haemophilus influenzae type b; Neisseria Meningitidis
Palabras clave
Versiones (1)
- 25/3/19 25/3/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
25 de marzo de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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GSK Biologicals' Hib-MenCY-TT Conjugate Vaccine vs ActHIB® & MenC Conjugate Licensed Vaccine (NCT00134719)
Study Conclusion
- StudyEvent: ODM
Descripción
Follow-Up Studies
Alias
- UMLS CUI-1
- C0016441
Descripción
Follow-up Study, Study Subject Participation Status
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
Descripción
Follow-up Study, Study Subject Participation Status, Reason
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0566251
Descripción
Follow-up Study, Study Subject Participation Status, Reason
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0566251
Descripción
Occurrence of Serious Adverse Event
Alias
- UMLS CUI-1
- C1519255
Descripción
Serious Adverse Event, During, Study
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C2603343
Descripción
Serious Adverse Event, Count of entities
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449788
Descripción
Elimination Criteria
Alias
- UMLS CUI-1
- C0680251
Descripción
Withdrawal
Alias
- UMLS CUI-1
- C2349954
Descripción
Patient withdrawn from trial
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0422727
Descripción
Patient withdrawn from trial, Indication
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C3146298
Descripción
Patient withdrawn from trial, Indication
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C3146298
Descripción
Patient withdrawn from trial, Decision maker
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
Descripción
Patient withdrawn from trial, Date last contact
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0805839
Descripción
Patient withdrawn from trial, Date last contact, Condition
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0805839
- UMLS CUI [1,3]
- C0348080
Descripción
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Descripción
I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator Signature, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Descripción
Investigator Name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826892
Similar models
Study Conclusion
- StudyEvent: ODM
C2348568 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C0449788 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,2])
C0805839 (UMLS CUI [1,2])
C0805839 (UMLS CUI [1,2])
C0348080 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])