ID

35780

Descrizione

Study ID: 110028 Clinical Study ID: 110028 Study Title: Study to Evaluate the Safety and Immune Response of Two-Doses of Candidate Influenza Vaccine GSK 1557484A in Adults Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00510874 https://clinicaltrials.gov/ct2/show/NCT00510874 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Candidate Influenza Vaccine Trade Name: Pumarix, Pandemrix Study Indication: Influenza This study consists of 6 Visits and one Telephone Contact: -Visit 1: Visit „Day 0“ -Visit 2: Visit „Day 7“, Contact Window: Day 6-8, Minimum Number of Days between Successive Visits: 6 -Visit 3: Visit „Day 21“: Contact Window: Day 19-23, Minimum Number of Days between Successive Visits: 12 -Visit 4: Visit „Day 28“: Contact Window: Day 26-30, Minimum Number of Days between Successive Visits: 6 -Visit 5: Visit „Day 42“: Contact Window: Day 38-46, Minimum Number of Days between S ccessive Visits: 12 -Telephone Contact „Day 84“: Contact Window: Day 80-88 -Visit 6: Visit „Day 182“: Contact Window: Day 167-197 The screening can take place up to 21 days prior to Visit 1. This document contains the Screening conclusion form. It has to be filled in after the screening visit.

collegamento

https://clinicaltrials.gov/ct2/show/NCT00510874

Keywords

versioni (2)
  1. 22/03/19 22/03/19 -
  2. 22/03/19 22/03/19 - Sarah Riepenhausen
Titolare del copyright

GlaxoSmithKline

Caricato su

22 marzo 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Safety and Immune Response of Two-Doses of Candidate Influenza Vaccine in Adults, NCT00510874

Inglese

Screening conclusion

1 moduli  
  1. StudyEvent: ODM
    1. Screening conclusion
Administrative data
Descrizione

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Number
Descrizione

Subject Number

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Date of Screening
Descrizione

day month year

Tipo di dati

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1710477
Screening conclusion
Descrizione

Screening conclusion

Alias
UMLS CUI-1
C1710477
UMLS CUI-2
C1707478
Did the subject experience any Serious Adverse Event during screening?
Descrizione

only SAEs related to study participation or to a concurrent medication need to be considered and reported.

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C1710477
If subject experienced any SAE during sceening period, please specify total number of SAEs.
Descrizione

SAE Number during screening

Tipo di dati

integer

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C0237753
UMLS CUI [1,3]
C1710477
Is the subject a screening failure?
Descrizione

Was the subject withdrawn prior to randomisation or first vaccination?

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0566251
If the subject was a screening failure, please tick the major reason for failure
Descrizione

(Tick one box only). If you tick ELI: Please tick failing criteria on Eligibility form. If you tick SAE: Please complete and submit SAE report. Please specify SAE No. in the "SAE Number" Item.

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0566251
Reason for failure in screening, specification
Descrizione

Specify if you ticked "Protocol violation" or "Other" as major reason for failure.

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0566251
Who made the decision?
Descrizione

Decision taken for screening failure

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1710476
UMLS CUI [1,2]
C0566251
UMLS CUI [1,3]
C0679006
Investigator's Signature
Descrizione

Investigator's Signature

Alias
UMLS CUI-1
C2346576
Investigator's signature
Descrizione

I confirm that I have reviewed the data in these screening forms 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 di dati

text

Alias
UMLS CUI [1]
C2346576
Printed Investigator's name
Descrizione

Printed Investigator's name

Tipo di dati

text

Alias
UMLS CUI [1]
C2826892
Date of signature
Descrizione

day month year

Tipo di dati

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
Ritorna all'inizio della pagina

Similar models

Screening conclusion

1 moduli
  1. StudyEvent: ODM
    1. Screening conclusion
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Date of Screening
Item
Date of Screening
date
C0011008 (UMLS CUI [1,1])
C1710477 (UMLS CUI [1,2])
Item Group
Screening conclusion
C1710477 (UMLS CUI-1)
C1707478 (UMLS CUI-2)
Item
Did the subject experience any Serious Adverse Event during screening?
text
C1519255 (UMLS CUI [1,1])
C1710477 (UMLS CUI [1,2])
SAE
Code List
Did the subject experience any Serious Adverse Event during screening?
CL Item
Yes (Y)
CL Item
No (N)
SAE Number during screening
Item
If subject experienced any SAE during sceening period, please specify total number of SAEs.
integer
C1519255 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C1710477 (UMLS CUI [1,3])
Item
Is the subject a screening failure?
text
C1710476 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Screening failure
Code List
Is the subject a screening failure?
CL Item
Yes (Y)
CL Item
No (N)
Item
If the subject was a screening failure, please tick the major reason for failure
text
C1710476 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Screening failure
Code List
If the subject was a screening failure, please tick the major reason for failure
CL Item
Eligibility criteria not fulfilled (inclusion and exclusion criteria) (ELI)
CL Item
Protocol violation (PTV)
CL Item
Serious adverse event (SAE)
CL Item
Consent withdrawal not due to a serious adverse event (CWS)
CL Item
Migrated / moved from the study area (MIG)
CL Item
Lost to follow-up (LFU)
CL Item
Other (OTH)
Reason for failure in screening, specification
Item
Reason for failure in screening, specification
text
C1710476 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Item
Who made the decision?
text
C1710476 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,3])
Decision taken
Code List
Who made the decision?
CL Item
Investigator (I)
CL Item
Subject (S)
Item Group
Investigator's Signature
C2346576 (UMLS CUI-1)
Investigator's signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1])
Printed Investigator's name
Item
Printed Investigator's name
text
C2826892 (UMLS CUI [1])
Date of signature
Item
Date of signature
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial