Eligibility Major Depression NCT01034995

Inclusion Criteria
Descrição

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).
Descrição

ID.1

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
inpatient hospitalization at screening
Descrição

ID.2

Tipo de dados

boolean

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

ID.3

Tipo de dados

boolean

significant suicide risk
Descrição

ID.4

Tipo de dados

boolean

mild depression as measured by standard clinical research scales
Descrição

ID.5

Tipo de dados

boolean

history of failure to respond to antidepressant treatment
Descrição

ID.6

Tipo de dados

boolean

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

ID.7

Tipo de dados

boolean

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

ID.8

Tipo de dados

boolean

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

ID.9

Tipo de dados

boolean

Similar models

Eligibility Major Depression NCT01034995

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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