ID

29018

Description

Study part: Subject Treatment Status (Unscheduled). 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.

Keywords

  1. 2/20/18 2/20/18 -
Copyright Holder

Roche

Uploaded on

February 20, 2018

DOI

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License

Creative Commons BY-NC 3.0

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Subject Treatment Status (Unscheduled) rhuFab V2 Neovascular Age-Related Macular Degeneration FVF2598g

Subject Treatment Status (Unscheduled)

SUBJECT TREATMENT STATUS (UNSCHEDULED)
Description

SUBJECT TREATMENT STATUS (UNSCHEDULED)

Alias
UMLS CUI-1
C0420207
Subject Number:
Description

Subject Number

Data type

text

Alias
UMLS CUI [1]
C2348585
Subject Initials:
Description

Subject Initials

Data type

text

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

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Date of Treatment Discontinuation:
Description

Date treatment stopped

Data type

date

Alias
UMLS CUI [1]
C1531784
PRIMARY reason for permanent treatment discontinuation:
Description

indication

Data type

text

Alias
UMLS CUI [1]
C3146298
Please specify intervention:
Description

Interventional procedure

Data type

text

Alias
UMLS CUI [1]
C0184661

Similar models

Subject Treatment Status (Unscheduled)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
SUBJECT TREATMENT STATUS (UNSCHEDULED)
C0420207 (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])
Date treatment stopped
Item
Date of Treatment Discontinuation:
date
C1531784 (UMLS CUI [1])
Item
PRIMARY reason for permanent treatment discontinuation:
text
C3146298 (UMLS CUI [1])
Code List
PRIMARY reason for permanent treatment discontinuation:
CL Item
Adverse Event (complete appropriate AE CRF) (Adverse Event (complete appropriate AE CRF))
C0877248 (UMLS CUI-1)
(Comment:en)
CL Item
Subject’s decision (for reason other than AE) (Subject’s decision (for reason other than AE))
C0422727 (UMLS CUI-1)
C0679006 (UMLS CUI-2)
(Comment:en)
CL Item
Physician’s decision (for reason other than AE) (Physician’s decision (for reason other than AE))
C1709536 (UMLS CUI-1)
(Comment:en)
CL Item
Subject’s condition mandated other therapeutic intervention (Subject’s condition mandated other therapeutic intervention)
C0184661 (UMLS CUI-1)
(Comment:en)
Interventional procedure
Item
Please specify intervention:
text
C0184661 (UMLS CUI [1])

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