Study Conclusion

  1. StudyEvent: ODM
    1. Study Conclusion
Administrative Data
Descrizione

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Descrizione

Clinical Trial Subject Unique Identifier

Tipo di dati

integer

Alias
UMLS CUI [1]
C2348585
Study Conclusion
Descrizione

Study Conclusion

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C1707478
Date of subject completion or withdrawal
Descrizione

Clinical Trials, End Date

Tipo di dati

date

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C0806020
Time of withdrawal
Descrizione

Clinical Trials, Withdraw, Time

Tipo di dati

time

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0040223
Was the subject withdrawn from the study?
Descrizione

Clinical Trials, Withdraw

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
If Yes, check the primary reason for withdrawal
Descrizione

Clinical Trials, Withdraw, Reason and justification

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0566251
Other, specify
Descrizione

Clinical Trials, Withdraw, Reason and justification

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0566251

Similar models

Study Conclusion

  1. StudyEvent: ODM
    1. Study Conclusion
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
Study Conclusion
C0008976 (UMLS CUI-1)
C1707478 (UMLS CUI-2)
Clinical Trials, End Date
Item
Date of subject completion or withdrawal
date
C0008976 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Clinical Trials, Withdraw, Time
Item
Time of withdrawal
time
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Clinical Trials, Withdraw
Item
Was the subject withdrawn from the study?
boolean
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
Item
If Yes, check the primary reason for withdrawal
text
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Code List
If Yes, check the primary reason for withdrawal
CL Item
Adverse event  (1)
CL Item
Lost to follow-up (2)
CL Item
Protocol violation (3)
CL Item
Subject decided to withdraw from the study  (4)
CL Item
Lack of efficacy (5)
CL Item
Sponsor terminated study (6)
CL Item
Other, specify (7)
Clinical Trials, Withdraw, Reason and justification
Item
Other, specify
text
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])