ID

29308

Description

Study part: Subset PK Sample Informed Consent Screening. A Phase III, Multicenter, Randomized, Sham Injection-Controlled Study Of The Efficacy And Safety Of Ranibizumab Injection Compared With Sham In Subjects with Macular Edema Secondary To Branch Retinal Vein Occlusion.

Mots-clés

  1. 18/03/2018 18/03/2018 -
Détendeur de droits

Roche

Téléchargé le

18 mars 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Subset PK Sample Informed Consent Screening Ranibizumab Macular Edema Secondary To Branch Retinal Vein Occlusion FVF4165g

Subset PK Sample Informed Consent Screening

Subset PK Sample Informed Consent Screening
Description

Subset PK Sample Informed Consent Screening

Alias
UMLS CUI-1
C0201734
UMLS CUI-2
C0370003
Subject number:
Description

Subject number

Type de données

text

Alias
UMLS CUI [1]
C2348585
Subject initials:
Description

Subject initials

Type de données

text

Alias
UMLS CUI [1,1]
C1997894
UMLS CUI [1,2]
C2986440
Visit date:
Description

Visit date

Type de données

date

Alias
UMLS CUI [1]
C1320303
Not Applicable (Subject not participating)
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
Date subject signed research sample informed consent:
Description

Informed Consent Date

Type de données

date

Alias
UMLS CUI [1]
C2985782

Similar models

Subset PK Sample Informed Consent Screening

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Subset PK Sample Informed Consent Screening
C0201734 (UMLS CUI-1)
C0370003 (UMLS CUI-2)
Subject number
Item
Subject number:
text
C2348585 (UMLS CUI [1])
Subject initials
Item
Subject initials:
text
C1997894 (UMLS CUI [1,1])
C2986440 (UMLS CUI [1,2])
Visit date
Item
Visit date:
date
C1320303 (UMLS CUI [1])
Study Subject Participation Status
Item
Not Applicable (Subject not participating)
boolean
C2348568 (UMLS CUI [1])
Informed Consent Date
Item
Date subject signed research sample informed consent:
date
C2985782 (UMLS CUI [1])

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