Eligibility Major Depressive Disorder NCT00385307

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient with major depressive disorder diagnosed according to diagnostic and statistical manual of mental disorders dsm-iv-tr
Beskrivning

Major Depressive Disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C1269683
patient meets criteria for a recurrent major depressive episode (mde)
Beskrivning

Recurrent major depressive episode

Datatyp

boolean

Alias
UMLS CUI [1]
C0154409
patient meets severity assessments of depression specified by the study
Beskrivning

Depressive disorder Severity Assessment | Severity Specified Study Protocol

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0011581
UMLS CUI [1,2]
C0439793
UMLS CUI [1,3]
C1516048
UMLS CUI [2,1]
C0439793
UMLS CUI [2,2]
C0205369
UMLS CUI [2,3]
C2348563
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient is at immediate risk for suicidal behavior
Beskrivning

Suicidal behavior At risk Immediate

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1760428
UMLS CUI [1,2]
C1444641
UMLS CUI [1,3]
C0205253
patient is with a unstable medical condition
Beskrivning

Medical condition Unstable

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0443343
patient with psychotic features, catatonic features, seasonal pattern or postpartum onset
Beskrivning

Psychotic symptom | Feature Catatonic | Seasonal Affective Disorder | Depression, Postpartum

Datatyp

boolean

Alias
UMLS CUI [1]
C0871189
UMLS CUI [2,1]
C2348519
UMLS CUI [2,2]
C0007398
UMLS CUI [3]
C0085159
UMLS CUI [4]
C0221074
patient has taken concomitant treatment that may interfere with valid collection or interpretation of study data
Beskrivning

Therapeutic procedure Interferes with Study data | Therapeutic procedure Interferes with Study data Interpretation

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0681873
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0681873
UMLS CUI [2,4]
C0459471
patient has been treated with non-pharmacologic therapy intended to treat depression in the past 6 months
Beskrivning

Therapeutic procedure Depressive disorder | Pharmaceutical Preparations Absent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0011581
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0332197
patient has been treated with paroxetine (paxil) within the previous 6 months
Beskrivning

Paroxetine | Paxil

Datatyp

boolean

Alias
UMLS CUI [1]
C0070122
UMLS CUI [2]
C0376414
patient is pregnant or breastfeeding, or likely to become pregnant during the course of the study
Beskrivning

Pregnancy | Breast Feeding | Pregnancy Expected

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0032961
UMLS CUI [3,2]
C1517001

Similar models

Eligibility Major Depressive Disorder NCT00385307

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
Item Group
C0680251 (UMLS CUI)
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])
Medical condition Unstable
Item
patient is with a unstable medical condition
boolean
C3843040 (UMLS CUI [1,1])
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])
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])
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])
Paroxetine | Paxil
Item
patient has been treated with paroxetine (paxil) within the previous 6 months
boolean
C0070122 (UMLS CUI [1])
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])