Eligibility Major Depression NCT01034995

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with a diagnosis of major depressive disorder, as defined by the diagnostic and statistical manual of mental disorders, 4th edition, text revision (dsm-iv-tr) criteria (296.3) and confirmed by the semi-structured mini international neuropsychiatric interview (mini).
Beskrivning

ID.1

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
inpatient hospitalization at screening
Beskrivning

ID.2

Datatyp

boolean

symptoms of depression present for <30 days or >2 years
Beskrivning

ID.3

Datatyp

boolean

significant suicide risk
Beskrivning

ID.4

Datatyp

boolean

mild depression as measured by standard clinical research scales
Beskrivning

ID.5

Datatyp

boolean

history of failure to respond to antidepressant treatment
Beskrivning

ID.6

Datatyp

boolean

other psychiatric conditions that could obscure the results of the study
Beskrivning

ID.7

Datatyp

boolean

for women of child-bearing potential, the unwillingness to use highly effective means of birth control
Beskrivning

ID.8

Datatyp

boolean

the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Beskrivning

ID.9

Datatyp

boolean

Similar models

Eligibility Major Depression NCT01034995

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with a diagnosis of major depressive disorder, as defined by the diagnostic and statistical manual of mental disorders, 4th edition, text revision (dsm-iv-tr) criteria (296.3) and confirmed by the semi-structured mini international neuropsychiatric interview (mini).
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
inpatient hospitalization at screening
boolean
ID.3
Item
symptoms of depression present for <30 days or >2 years
boolean
ID.4
Item
significant suicide risk
boolean
ID.5
Item
mild depression as measured by standard clinical research scales
boolean
ID.6
Item
history of failure to respond to antidepressant treatment
boolean
ID.7
Item
other psychiatric conditions that could obscure the results of the study
boolean
ID.8
Item
for women of child-bearing potential, the unwillingness to use highly effective means of birth control
boolean
ID.9
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean