ID

28972

Description

Study part: Follow- up Contact Month 3. A Phase III, Multicenter, Randomized, Double-Masked, Sham Injection-Controlled Study Of The Efficacy And Safety Of rhuFab V2 (Ranibizumab) In Subjects With Minimally Classic Or Occult Subfoveal Neovascular Age-Related Macular Degeneration.

Mots-clés

  1. 18/02/2018 18/02/2018 -
Détendeur de droits

Roche

Téléchargé le

18 février 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Follow- up Contact Month 3 rhuFab V2 Neovascular Age-Related Macular Degeneration FVF2598g

Follow- up Contact Month 3

FOLLOW-UP CONTACT (MONTH 3)
Description

FOLLOW-UP CONTACT (MONTH 3)

Alias
UMLS CUI-1
C1522577
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

text

Alias
UMLS CUI [1]
C1320303
Was the subject contacted 2 days after study treatment?
Description

follow-up visit

Type de données

boolean

Alias
UMLS CUI [1]
C0589121
Date of Contact:
Description

Date of Contact

Type de données

date

Alias
UMLS CUI [1]
C0805839
Has the subject been taking the prescribed self-administered post-injection antimicrobials?
Description

post treatment antibodies

Type de données

boolean

Alias
UMLS CUI [1,1]
C2709088
UMLS CUI [1,2]
C0003241
Decrease in Vision- Has the subject experienced a decrease in vision in the study eye since treatment?
Description

Low Vision

Type de données

boolean

Alias
UMLS CUI [1]
C0042798
Eye Pain- Has the subject had any eye pain in the study eye since treatment?
Description

Eye Pain

Type de données

boolean

Alias
UMLS CUI [1]
C0151827
Unusual Redness- Has the subject had any new or unusual redness in the study eye (other than localized redness at the injection site) since treatment?
Description

eye redness

Type de données

boolean

Alias
UMLS CUI [1]
C0235267
New Ocular Symptoms- Has the subject experienced any other new ocular symptoms in the study eye since treatment?
Description

Ocular Symptoms

Type de données

boolean

Alias
UMLS CUI [1]
C0586406
Safety Assessment Visit- Was the subject asked to return to the clinic for a safety assessment visit?
Description

Safety Assessment Visit

Type de données

boolean

Alias
UMLS CUI [1,1]
C0589121
UMLS CUI [1,2]
C0549076

Similar models

Follow- up Contact Month 3

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
FOLLOW-UP CONTACT (MONTH 3)
C1522577 (UMLS CUI-1)
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:
text
C1320303 (UMLS CUI [1])
follow-up visit
Item
Was the subject contacted 2 days after study treatment?
boolean
C0589121 (UMLS CUI [1])
Date of Contact
Item
Date of Contact:
date
C0805839 (UMLS CUI [1])
post treatment antibodies
Item
Has the subject been taking the prescribed self-administered post-injection antimicrobials?
boolean
C2709088 (UMLS CUI [1,1])
C0003241 (UMLS CUI [1,2])
Low Vision
Item
Decrease in Vision- Has the subject experienced a decrease in vision in the study eye since treatment?
boolean
C0042798 (UMLS CUI [1])
Eye Pain
Item
Eye Pain- Has the subject had any eye pain in the study eye since treatment?
boolean
C0151827 (UMLS CUI [1])
eye redness
Item
Unusual Redness- Has the subject had any new or unusual redness in the study eye (other than localized redness at the injection site) since treatment?
boolean
C0235267 (UMLS CUI [1])
Ocular Symptoms
Item
New Ocular Symptoms- Has the subject experienced any other new ocular symptoms in the study eye since treatment?
boolean
C0586406 (UMLS CUI [1])
Safety Assessment Visit
Item
Safety Assessment Visit- Was the subject asked to return to the clinic for a safety assessment visit?
boolean
C0589121 (UMLS CUI [1,1])
C0549076 (UMLS CUI [1,2])

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