Patient Continuation

  1. StudyEvent: ODM
    1. Patient Continuation
Patient Continuation
Descripción

Patient Continuation

Alias
UMLS CUI-1
C2348568
Is the patient continuing in the study?
Descripción

Patient Continuation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
If ’No’, please mark the primary cause of withdrawal. (Mark one box only).
Descripción

primary cause of withdrawal

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Primary cause of withdrawal: If 'Other', please specify
Descripción

primary cause of withdrawal

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Investigator’s Signature
Descripción

Investigator’s Signature

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Investigator’s Signature Date
Descripción

Investigator’s Signature Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008

Similar models

Patient Continuation

  1. StudyEvent: ODM
    1. Patient Continuation
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Patient Continuation
C2348568 (UMLS CUI-1)
Patient Continuation
Item
Is the patient continuing in the study?
boolean
C2348568 (UMLS CUI [1])
Item
If ’No’, please mark the primary cause of withdrawal. (Mark one box only).
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
If ’No’, please mark the primary cause of withdrawal. (Mark one box only).
CL Item
Baseline sign and symptom  (1)
CL Item
Does not meet inclusion/exclusion criteria (2)
CL Item
Protocol deviation (including non-compliance) (3)
CL Item
Lost to follow-up (4)
CL Item
Other (5)
primary cause of withdrawal
Item
Primary cause of withdrawal: If 'Other', please specify
text
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Investigator’s Signature
Item
Investigator’s Signature
text
C2346576 (UMLS CUI [1])
Investigator’s Signature Date
Item
Investigator’s Signature Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])