ID
27525
Description
Study Part: Appendices. TMP001 in Relapsing-remitting Multiple Sclerosis: A Multicentre Open, Baseline-controlled Phase IIa Clinical Trial.
Keywords
Versions (1)
- 11/19/17 11/19/17 -
Copyright Holder
SocraMetrics
Uploaded on
November 19, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Appendices TMP001 Multiple Sclerosis NCT02686788
Appendices
- StudyEvent: ODM
Description
Begleiterkrankungen
Alias
- UMLS CUI-1
- C0009488
Description
Comorbidity
Data type
text
Alias
- UMLS CUI [1]
- C0009488
Description
Comorbidity
Data type
text
Alias
- UMLS CUI [1]
- C0009488
Description
Start date
Data type
partialDate
Alias
- UMLS CUI [1]
- C0808070
Description
Ongoing
Data type
boolean
Alias
- UMLS CUI [1]
- C2826680
Description
End date
Data type
partialDate
Alias
- UMLS CUI [1]
- C0806020
Description
Medikation
Alias
- UMLS CUI-1
- C0013227
Description
Medication name
Data type
text
Alias
- UMLS CUI [1]
- C2360065
Description
Indication
Data type
text
Alias
- UMLS CUI [1]
- C3146298
Description
Adverse events
Data type
text
Alias
- UMLS CUI [1]
- C0877248
Description
Other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
Dosage
Data type
text
Alias
- UMLS CUI [1]
- C3174092
Description
Frequency
Data type
text
Alias
- UMLS CUI [1]
- C3476109
Description
other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
dosage form
Data type
text
Alias
- UMLS CUI [1]
- C0013058
Description
application routes
Data type
text
Alias
- UMLS CUI [1]
- C0013153
Description
start date
Data type
date
Alias
- UMLS CUI [1]
- C0808070
Description
Ongoing
Data type
boolean
Alias
- UMLS CUI [1]
- C2826680
Description
End date
Data type
date
Alias
- UMLS CUI [1]
- C0806020
Description
MS-Schübe
Alias
- UMLS CUI-1
- C0581392
Description
Start date
Data type
date
Alias
- UMLS CUI [1]
- C0808070
Description
End date
Data type
date
Alias
- UMLS CUI [1]
- C0806020
Description
Therapy Exacerbation of multiple sclerosis
Data type
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0581392
Description
Other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
Unerwünschte Ereignisse/ Adverse Events
Alias
- UMLS CUI-1
- C0877248
Description
Adverse Events
Data type
text
Alias
- UMLS CUI [1]
- C0877248
Description
Adverse Events
Data type
text
Alias
- UMLS CUI [1]
- C0877248
Description
Start date
Data type
date
Alias
- UMLS CUI [1]
- C0808070
Description
Ongoing
Data type
boolean
Alias
- UMLS CUI [1]
- C2826680
Description
End date
Data type
date
Alias
- UMLS CUI [1]
- C0806020
Description
Seriousness
Data type
text
Alias
- UMLS CUI [1]
- C1710056
Description
intensity
Data type
text
Alias
- UMLS CUI [1]
- C1710066
Description
Action taken
Data type
text
Alias
- UMLS CUI [1]
- C2826626
Description
Other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
Causality of AE
Data type
text
Alias
- UMLS CUI [1]
- C3641099
Description
Outcome
Data type
text
Alias
- UMLS CUI [1]
- C1705586
Description
Zusätzliche Untersuchungen/ Nachverfolgung von Unerwünschten Ereignissen
Alias
- UMLS CUI-1
- C1522577
Description
visit date
Data type
date
Alias
- UMLS CUI [1]
- C1320303
Description
Indication
Data type
text
Alias
- UMLS CUI [1]
- C3146298
Description
adverse events
Data type
text
Alias
- UMLS CUI [1]
- C0877248
Description
other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
Result
Data type
text
Alias
- UMLS CUI [1]
- C1274040
Description
other
Data type
text
Alias
- UMLS CUI [1]
- C0205394
Description
Laboratory test result abnormal
Data type
text
Alias
- UMLS CUI [1]
- C0438215
Similar models
Appendices
- StudyEvent: ODM
C0581392 (UMLS CUI [1,2])