ID

24902

Description

Study ID: 100571 (M138) Clinical Study ID: 100571 Study Title: Double-blind randomized study to evaluate the immunogenicity and reactogenicity of two different lots of GlaxoSmithKline Biologicals' inactivated hepatitis A vaccine containing 1440 EL.U of antigen per mL and injected according to a 0, 12 month schedule in healthy adult volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00291876 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 4 Study Recruitment Status: Completed Generic Name: Hepatitis A Vaccine, Inactivated Trade Name: Havrix Study Indication: Hepatitis A https://clinicaltrials.gov/ct2/show/NCT00291876

Lien

https://clinicaltrials.gov/ct2/show/NCT00291876

Mots-clés

  1. 22/08/2017 22/08/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

22 août 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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GSK Hepatitis A Vaccine Month 174 Visit 21 DEMOGRAPHICS NCT00291876

GSK Hepatitis A Vaccine Month 174 Visit 21 DEMOGRAPHICS NCT00291876

Study administration
Description

Study administration

Center
Description

Center

Type de données

text

Alias
UMLS CUI [1,1]
C1301943 (Institution name)
SNOMED
398321007
UMLS CUI [1,2]
C0600091 (Identifier)
SNOMED
118522005
LOINC
LP31795-5
Date of Visit
Description

Date of Visit

Type de données

date

Alias
UMLS CUI [1]
C1320303 (Date of visit)
SNOMED
406543005
Subject Number
Description

Subject Identifier

Type de données

integer

Alias
UMLS CUI [1]
C2348585 (Clinical Trial Subject Unique Identifier)
DEMOGRAPHICS
Description

DEMOGRAPHICS

I certify that Informed Consent has been obtained prior to any study procedure. Informed Consent Date:
Description

Informed Consent Date

Type de données

date

Alias
UMLS CUI [1]
C2985782 (Informed Consent Date)
Subject Initials
Description

Subject Initials

Type de données

text

Unités de mesure
  • _ _ First Name / _ _ Family Name
Alias
UMLS CUI [1]
C2986440 (Person Initials)
_ _ First Name / _ _ Family Name
Date of Birth
Description

Date of Birth

Type de données

date

Alias
UMLS CUI [1]
C0421451 (Patient date of birth)
SNOMED
184099003
LOINC
LP57552-9
Gender
Description

Gender

Type de données

integer

Alias
UMLS CUI [1]
C0079399 (Gender)
SNOMED
263495000
LOINC
LP61312-2
Race
Description

Race

Type de données

text

Alias
UMLS CUI [1]
C0034510 (Racial group)
SNOMED
415229000
LOINC
LP7528-5
If Other, please specify
Description

other Race

Type de données

text

Alias
UMLS CUI [1]
C0034510 (Racial group)
SNOMED
415229000
LOINC
LP7528-5

Similar models

GSK Hepatitis A Vaccine Month 174 Visit 21 DEMOGRAPHICS NCT00291876

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Study administration
Center
Item
Center
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Subject Identifier
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Item Group
DEMOGRAPHICS
Informed Consent Date
Item
I certify that Informed Consent has been obtained prior to any study procedure. Informed Consent Date:
date
C2985782 (UMLS CUI [1])
Subject Initials
Item
Subject Initials
text
C2986440 (UMLS CUI [1])
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Gender
integer
C0079399 (UMLS CUI [1])
Code List
Gender
CL Item
Male (1)
CL Item
Female (2)
Item
Race
text
C0034510 (UMLS CUI [1])
Code List
Race
CL Item
White (WH)
CL Item
Black (BL)
CL Item
Oriental (OR)
CL Item
Other, please specify (OT)
other Race
Item
If Other, please specify
text
C0034510 (UMLS CUI [1])

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