ID
29749
Description
https://clinicaltrials.gov/show/NCT00197028 Visit 1 Case Report Form Study ID: 103967 Clinical Study ID: 103967 Study Title: A Phase I/IIb randomized, double-blind, controlled study of the safety, immunogenicity and proof-of-concept of RTS,S/AS02D, a candidate malaria vaccine in infants living in a malaria-endemic region Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00197028 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: SB257049 Trade Name: BIO MALARIA; SB257049 Study Indication: Malaria
Lien
https://clinicaltrials.gov/show/NCT00197028
Mots-clés
Versions (1)
- 18/04/2018 18/04/2018 -
Détendeur de droits
GlaxoSmithKline (GSK)
Téléchargé le
18 avril 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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RTS,S/AS02D, a candidate malaria vaccine in infants living in a malaria-endemic region, Study ID: 103967, NCT00197028
Case Report Form, Screening, Visit 1
- StudyEvent: ODM
Description
Informed Consent and Demographics
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C0011298
Description
Informed Consent Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0021430
Description
Center Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0600091
Description
Date of birth
Type de données
date
Alias
- UMLS CUI [1]
- C0421451
Description
Gender
Type de données
text
Alias
- UMLS CUI [1]
- C0079399
Description
Race
Type de données
integer
Alias
- UMLS CUI [1]
- C0034510
Description
Geographical area
Type de données
integer
Alias
- UMLS CUI [1]
- C0681784
Description
Eligibility Check
Alias
- UMLS CUI-1
- C0013893
Description
Do not enter the subject into the study if he/she failed any inclusion or exclusion criteria below.
Type de données
integer
Alias
- UMLS CUI [1]
- C0013893
Description
Inclusion criteria
Type de données
integer
Description
Exclusion Criteria
Type de données
integer
Description
Screening conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008976
- UMLS CUI-3
- C0042210
Description
Serious Adverse Event
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
Description
Number of SAEs
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0449788
- UMLS CUI [1,2]
- C1519255
Description
Screening failure
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1710477
- UMLS CUI [1,2]
- C0231175
Description
Screening failure
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1710477
- UMLS CUI [1,2]
- C0231175
Description
Decision maker
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
Description
Administative data
Alias
- UMLS CUI-1
- C1320722
Description
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.
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Description
Printed name
Type de données
text
Alias
- UMLS CUI [1]
- C2826892
Similar models
Case Report Form, Screening, Visit 1
- StudyEvent: ODM
C0011298 (UMLS CUI-2)
C0021430 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0008976 (UMLS CUI-2)
C0042210 (UMLS CUI-3)
C1519255 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])