ID
35813
Beschreibung
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
Stichworte
Versionen (1)
- 25.03.19 25.03.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
25. März 2019
DOI
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Lizenz
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
Beschreibung
Follow-Up Studies
Alias
- UMLS CUI-1
- C0016441
Beschreibung
Follow-up Study, Study Subject Participation Status
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
Beschreibung
Follow-up Study, Study Subject Participation Status, Reason
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0566251
Beschreibung
Follow-up Study, Study Subject Participation Status, Reason
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0016441
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0566251
Beschreibung
Occurrence of Serious Adverse Event
Alias
- UMLS CUI-1
- C1519255
Beschreibung
Serious Adverse Event, During, Study
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C2603343
Beschreibung
Serious Adverse Event, Count of entities
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449788
Beschreibung
Elimination Criteria
Alias
- UMLS CUI-1
- C0680251
Beschreibung
Withdrawal
Alias
- UMLS CUI-1
- C2349954
Beschreibung
Patient withdrawn from trial
Datentyp
text
Alias
- UMLS CUI [1]
- C0422727
Beschreibung
Patient withdrawn from trial, Indication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C3146298
Beschreibung
Patient withdrawn from trial, Indication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C3146298
Beschreibung
Patient withdrawn from trial, Decision maker
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
Beschreibung
Patient withdrawn from trial, Date last contact
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0805839
Beschreibung
Patient withdrawn from trial, Date last contact, Condition
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0805839
- UMLS CUI [1,3]
- C0348080
Beschreibung
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Investigator Signature, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beschreibung
Investigator Name
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Ähnliche Modelle
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])