Informatie:
Fout:
ID
21817
Beschrijving
Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder (SIRIUS); ODM derived from: https://clinicaltrials.gov/show/NCT00385307
Link
https://clinicaltrials.gov/show/NCT00385307
Trefwoorden
Versies (1)
- 02-05-17 02-05-17 -
Geüploaded op
2 mei 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT00385307
Eligibility Major Depressive Disorder NCT00385307
- StudyEvent: Eligibility
Similar models
Eligibility Major Depressive Disorder NCT00385307
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Major Depressive Disorder
Item
patient with major depressive disorder diagnosed according to diagnostic and statistical manual of mental disorders dsm-iv-tr
boolean
C1269683 (UMLS CUI [1])
Recurrent major depressive episode
Item
patient meets criteria for a recurrent major depressive episode (mde)
boolean
C0154409 (UMLS CUI [1])
Depressive disorder Severity Assessment | Severity Specified Study Protocol
Item
patient meets severity assessments of depression specified by the study
boolean
C0011581 (UMLS CUI [1,1])
C0439793 (UMLS CUI [1,2])
C1516048 (UMLS CUI [1,3])
C0439793 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C2348563 (UMLS CUI [2,3])
C0439793 (UMLS CUI [1,2])
C1516048 (UMLS CUI [1,3])
C0439793 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C2348563 (UMLS CUI [2,3])
Suicidal behavior At risk Immediate
Item
patient is at immediate risk for suicidal behavior
boolean
C1760428 (UMLS CUI [1,1])
C1444641 (UMLS CUI [1,2])
C0205253 (UMLS CUI [1,3])
C1444641 (UMLS CUI [1,2])
C0205253 (UMLS CUI [1,3])
Medical condition Unstable
Item
patient is with a unstable medical condition
boolean
C3843040 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,2])
Psychotic symptom | Feature Catatonic | Seasonal Affective Disorder | Depression, Postpartum
Item
patient with psychotic features, catatonic features, seasonal pattern or postpartum onset
boolean
C0871189 (UMLS CUI [1])
C2348519 (UMLS CUI [2,1])
C0007398 (UMLS CUI [2,2])
C0085159 (UMLS CUI [3])
C0221074 (UMLS CUI [4])
C2348519 (UMLS CUI [2,1])
C0007398 (UMLS CUI [2,2])
C0085159 (UMLS CUI [3])
C0221074 (UMLS CUI [4])
Therapeutic procedure Interferes with Study data | Therapeutic procedure Interferes with Study data Interpretation
Item
patient has taken concomitant treatment that may interfere with valid collection or interpretation of study data
boolean
C0087111 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0681873 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0681873 (UMLS CUI [2,3])
C0459471 (UMLS CUI [2,4])
C0521102 (UMLS CUI [1,2])
C0681873 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0681873 (UMLS CUI [2,3])
C0459471 (UMLS CUI [2,4])
Therapeutic procedure Depressive disorder | Pharmaceutical Preparations Absent
Item
patient has been treated with non-pharmacologic therapy intended to treat depression in the past 6 months
boolean
C0087111 (UMLS CUI [1,1])
C0011581 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0011581 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Paroxetine | Paxil
Item
patient has been treated with paroxetine (paxil) within the previous 6 months
boolean
C0070122 (UMLS CUI [1])
C0376414 (UMLS CUI [2])
C0376414 (UMLS CUI [2])
Pregnancy | Breast Feeding | Pregnancy Expected
Item
patient is pregnant or breastfeeding, or likely to become pregnant during the course of the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C1517001 (UMLS CUI [3,2])
C0006147 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C1517001 (UMLS CUI [3,2])