VX-950HPC3006 NCT01571583 Eligibility

Eligibility
Beschreibung

Eligibility

Does the subject meet all eligibility criteria for the trial?
Beschreibung

eligibility criteria

Datentyp

boolean

Alias
UMLS CUI [1]
C0013893
If nom please list the number of inclusion criteria not met (if applicable)
Beschreibung

inclusion criteria

Datentyp

text

Alias
UMLS CUI [1]
C1512693
If no, please list the number of exclusion criteria not met (if applicable)
Beschreibung

exclusion criteria

Datentyp

text

Alias
UMLS CUI [1]
C0680251
Please provide the date of protocol in effect at the time of screening
Beschreibung

date of protocol at time of screening

Datentyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0220908
Is the subject a screening failure?
Beschreibung

If yes, please complete the question below (reason for withdrawal)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1710477
UMLS CUI [1,2]
C0680095
Reason for withdrawal from study
Beschreibung

Reason for withdrawal from study

Subject did not fullfill all inclusion/exlusion criteria
Beschreibung

inclusion/exclusion criteria

Datentyp

boolean

Alias
UMLS CUI [1]
C1512693
UMLS CUI [2]
C0680251
adverse event related event, please specify
Beschreibung

(including death, abnormal lab values, intercurrent illness and pregnancy)

Datentyp

text

Alias
UMLS CUI [1]
C0877248
Subject lost to follow-up. Date of last contact with subject (visit, call...) in this trial
Beschreibung

Date of last contact with subject

Datentyp

date

Alias
UMLS CUI [1,1]
C0805839
UMLS CUI [1,2]
C0681850
Subject withdrew consent. Date consent withdrawn
Beschreibung

date consent withdrawn

Datentyp

date

Alias
UMLS CUI [1,1]
C1707492
UMLS CUI [1,2]
C0011008
subject non-compliant
Beschreibung

subject non-compliant

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0457432
UMLS CUI [1,2]
C0681850
sponsor's decision
Beschreibung

sponsor's decision

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2347796
UMLS CUI [1,2]
C0679006
other, please specify
Beschreibung

other reason

Datentyp

text

Alias
UMLS CUI [1]
C3840932

Ähnliche Modelle

VX-950HPC3006 NCT01571583 Eligibility

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Eligibility
eligibility criteria
Item
Does the subject meet all eligibility criteria for the trial?
boolean
C0013893 (UMLS CUI [1])
inclusion criteria
Item
If nom please list the number of inclusion criteria not met (if applicable)
text
C1512693 (UMLS CUI [1])
exclusion criteria
Item
If no, please list the number of exclusion criteria not met (if applicable)
text
C0680251 (UMLS CUI [1])
date of protocol at time of screening
Item
Please provide the date of protocol in effect at the time of screening
date
C0011008 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0220908 (UMLS CUI [2])
screening failure
Item
Is the subject a screening failure?
boolean
C1710477 (UMLS CUI [1,1])
C0680095 (UMLS CUI [1,2])
Item Group
Reason for withdrawal from study
inclusion/exclusion criteria
Item
Subject did not fullfill all inclusion/exlusion criteria
boolean
C1512693 (UMLS CUI [1])
C0680251 (UMLS CUI [2])
adverse event
Item
adverse event related event, please specify
text
C0877248 (UMLS CUI [1])
Date of last contact with subject
Item
Subject lost to follow-up. Date of last contact with subject (visit, call...) in this trial
date
C0805839 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
date consent withdrawn
Item
Subject withdrew consent. Date consent withdrawn
date
C1707492 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
subject non-compliant
Item
subject non-compliant
boolean
C0457432 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
sponsor's decision
Item
sponsor's decision
boolean
C2347796 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
other reason
Item
other, please specify
text
C3840932 (UMLS CUI [1])