ID
13042
Description
Observational Study to Assess a 6-months Treatment With Gladem; ODM derived from: https://clinicaltrials.gov/show/NCT02231268
Link
https://clinicaltrials.gov/show/NCT02231268
Keywords
Versions (1)
- 1/12/16 1/12/16 -
Uploaded on
January 12, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Depressive Disorder NCT02231268
Eligibility Depressive Disorder NCT02231268
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
hypersensitivity
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0074393
Description
concomitant treatment
Data type
boolean
Alias
- UMLS CUI [1]
- C1707479
Description
concomitant treatment
Data type
boolean
Alias
- UMLS CUI [1]
- C1707479
Description
epilepsy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0014544
- UMLS CUI [1,2]
- C0443343
Description
precaution
Data type
boolean
Alias
- UMLS CUI [1]
- C1882442
Description
epilepsy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0014544
- UMLS CUI [1,2]
- C0205360
Description
liver dysfunction
Data type
boolean
Alias
- UMLS CUI [1]
- C0086565
Description
suicidal
Data type
boolean
Alias
- UMLS CUI [1]
- C0438696
Description
sleeping disorders, emotional state
Data type
boolean
Alias
- UMLS CUI [1]
- C0037317
- UMLS CUI [2]
- C0935620
Description
pregnancy, lactation, contraception
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3]
- C0700589
Similar models
Eligibility Depressive Disorder NCT02231268
- StudyEvent: Eligibility
C0001779 (UMLS CUI [2])
C0074393 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,2])
C0935620 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])