ID

28962

Description

Study part: Study Drug Administration Day 0. 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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Study Drug Administration Day 0 rhuFab V2 Neovascular Age-Related Macular Degeneration FVF2598g

Study Drug Administration Day 0

STUDY DRUG ADMINISTRATION (DAY 0)
Description

STUDY DRUG ADMINISTRATION (DAY 0)

Alias
UMLS CUI-1
C3469597
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
Chosen Study Eye:
Description

Eye

Type de données

text

Alias
UMLS CUI [1]
C0015392
Was treatment (rhuFab V2 or sham procedure) administered?
Description

Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
If Yes, Record kit # administered:
Description

identification number

Type de données

text

Alias
UMLS CUI [1]
C1300638
Date Administered:
Description

Date Administered

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1533734
Time Administered:
Description

Time Administered

Type de données

time

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C1533734
Was lidocaine injection administered?
Description

Drug Administration lidocaine

Type de données

boolean

Alias
UMLS CUI [1,1]
C3469597
UMLS CUI [1,2]
C0023660
Were preoperative antimicrobials given?
Description

preoperative antimicrobials

Type de données

boolean

Alias
UMLS CUI [1]
C2114165

Similar models

Study Drug Administration Day 0

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
STUDY DRUG ADMINISTRATION (DAY 0)
C3469597 (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:
date
C1320303 (UMLS CUI [1])
Item
Chosen Study Eye:
text
C0015392 (UMLS CUI [1])
Code List
Chosen Study Eye:
CL Item
Right Eye (Right Eye)
C0229089 (UMLS CUI-1)
(Comment:en)
CL Item
Left Eye (Left Eye)
C0229090 (UMLS CUI-1)
(Comment:en)
Therapy
Item
Was treatment (rhuFab V2 or sham procedure) administered?
boolean
C0087111 (UMLS CUI [1])
identification number
Item
If Yes, Record kit # administered:
text
C1300638 (UMLS CUI [1])
Date Administered
Item
Date Administered:
date
C0011008 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
Time Administered
Item
Time Administered:
time
C0040223 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
Drug Administration lidocaine
Item
Was lidocaine injection administered?
boolean
C3469597 (UMLS CUI [1,1])
C0023660 (UMLS CUI [1,2])
preoperative antimicrobials
Item
Were preoperative antimicrobials given?
boolean
C2114165 (UMLS CUI [1])

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