ID

36310

Descripción

Study ID: 111258 Clinical Study ID: 111258 Study Title: A phase IV, observer-blind, randomized single-dose post-marketing study to compare the safety and immunogenicity of Fluviral Trivalent Split Virion Influenza Vaccine (2007 - 2008 Season) made with new vs. aged bulk material, in adults ranging in age from 18 to 60 Years. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00586469 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Influenza Vaccine Trade Name: Fluviral Study Indication: Influenza

Palabras clave

Versiones (1)
  1. 2/5/19 2/5/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

2 de mayo de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Fluvial Trivalent Split Vision Influenza Vaccine; NCT00586469

Inglés

Use of Human Samples by GSK

1 formularios  
Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Centre
Descripción

Study Coordinating Centre

Tipo de datos

text

Alias
UMLS CUI [1]
C2825181
Use of Human Samples by GSK
Descripción

Use of Human Samples by GSK

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0457083
In addition to the use of samples for the tests described in the protocol, samples might be used for other research by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
Descripción

Laboratory Procedures, Usage

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0457083
Please tick below box if a 15 years GSK storage period is covered by the subjectís Informed Consent form of your center.
Descripción

Laboratory Procedures, Storage, Duration

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C1698986
UMLS CUI [1,3]
C0449238
ICF Effective date
Descripción

Pharmaceutical Procedures, Usage, Informed Consent, Date in time

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0457083
UMLS CUI [1,3]
C0021430
UMLS CUI [1,4]
C0011008
Investigator's Signature
Descripción

Investigator's Signature

Alias
UMLS CUI-1
C2346576
Investigator's signature
Descripción

Investigator Signature

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Date
Descripción

Investigator Signature, Date in time

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
Printed Investigator's name
Descripción

Investigator Name

Tipo de datos

text

Alias
UMLS CUI [1]
C2826892
Volver a la parte superior de la página

Similar models

Use of Human Samples by GSK

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study Coordinating Centre
Item
Centre
text
C2825181 (UMLS CUI [1])
Item Group
Use of Human Samples by GSK
C0022885 (UMLS CUI-1)
C0457083 (UMLS CUI-2)
Item
In addition to the use of samples for the tests described in the protocol, samples might be used for other research by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
text
C0022885 (UMLS CUI [1,1])
C0457083 (UMLS CUI [1,2])
Laboratory Procedures, Usage
Code List
In addition to the use of samples for the tests described in the protocol, samples might be used for other research by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
CL Item
Quality Assurance of tests described in the protocol. This may include the management of the quality of these current tests, the maintenance or improvement of these current tests, the development of new test methods for the markers described in the protocol as well as making sure that new tests are comparable to previous methods and work reliably. (1)
CL Item
Further investigation by GSK Biologicals into the ability of Fluviral vaccine to protect people if any findings from related studies require it and further research in Influenza disease under study. These investigations excludes genetics and HIV testing. (2)
CL Item
Further investigation by GSK Biologicals into the ability of Fluviral vaccine to protect people if any findings from related studies require it and further research in Influenza disease under study. These investigations excludes genetics and HIV testing. (3)
CL Item
Further research by GSK Biologicals that is NOT RELATED to Fluviral vaccine or Influenza disease under study done on an anonymous basis (meaning that any identification linking (4)
CL Item
he subject to the sample is destroyed). This research excludes genetic and HIV testing and does not affect subject participation in the study. (he subject to the sample is destroyed). This research excludes genetic and HIV testing and does not affect subject participation in the study.)
Item
Please tick below box if a 15 years GSK storage period is covered by the subjectís Informed Consent form of your center.
text
C0022885 (UMLS CUI [1,1])
C1698986 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Laboratory Procedures, Storage, Duration
Code List
Please tick below box if a 15 years GSK storage period is covered by the subjectís Informed Consent form of your center.
CL Item
At least 15 years storage period by GSK Biologicals (1)
CL Item
Other, specify (2)
Pharmaceutical Procedures, Usage, Informed Consent, Date in time
Item
ICF Effective date
date
C0022885 (UMLS CUI [1,1])
C0457083 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item Group
Investigator's Signature
C2346576 (UMLS CUI-1)
Investigator Signature
Item
Investigator's signature
text
C2346576 (UMLS CUI [1])
Investigator Signature, Date in time
Item
Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Investigator Name
Item
Printed Investigator's name
text
C2826892 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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