Eligibility Major Depressive Disorder With Panic Attacks NCT00206765

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females, ages 21-55.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
ability to sign an informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
diagnosis of panic disorder, or mdd with panic attacks, single episode, recurrent, or chronic
Description

Panic Disorder | Major Depressive Disorder Associated with Panic Attacks | Single major depressive episode Recurrent | Chronic major depressive disorder, single episode

Data type

boolean

Alias
UMLS CUI [1]
C0030319
UMLS CUI [2,1]
C1269683
UMLS CUI [2,2]
C0332281
UMLS CUI [2,3]
C0086769
UMLS CUI [3,1]
C0024517
UMLS CUI [3,2]
C2945760
UMLS CUI [4]
C0520666
ham-a score >17
Description

Hamilton Anxiety Rating Scale Questionnaire

Data type

boolean

Alias
UMLS CUI [1]
C3541258
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
alcohol or substance abuse within the last 6 months
Description

Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0038586
current diagnosis of obsessive-compulsive disorder
Description

Obsessive-Compulsive Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0028768
current diagnosis of schizophrenia, schizoaffective disorder, or bipolar mood disorder
Description

Schizophrenia | Schizoaffective Disorder | Bipolar Mood Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
UMLS CUI [3]
C0005586
use of antipsychotic medications over the two months preceding enrollment in the study
Description

Antipsychotic Agents

Data type

boolean

Alias
UMLS CUI [1]
C0040615
changes in antidepressant or mood stabilizer dosing over the two months preceding enrollment in the study
Description

Antidepressive Agents Dosage altered | Mood Stabilizer Dosage altered

Data type

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C0420247
UMLS CUI [2,1]
C2917435
UMLS CUI [2,2]
C0420247
previous adverse reaction to risperidone or paroxetine.
Description

Adverse reaction Risperidone | Adverse reaction Paroxetine

Data type

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0073393
UMLS CUI [2,1]
C0559546
UMLS CUI [2,2]
C0070122

Similar models

Eligibility Major Depressive Disorder With Panic Attacks NCT00206765

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
males and females, ages 21-55.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
ability to sign an informed consent
boolean
C0021430 (UMLS CUI [1])
Panic Disorder | Major Depressive Disorder Associated with Panic Attacks | Single major depressive episode Recurrent | Chronic major depressive disorder, single episode
Item
diagnosis of panic disorder, or mdd with panic attacks, single episode, recurrent, or chronic
boolean
C0030319 (UMLS CUI [1])
C1269683 (UMLS CUI [2,1])
C0332281 (UMLS CUI [2,2])
C0086769 (UMLS CUI [2,3])
C0024517 (UMLS CUI [3,1])
C2945760 (UMLS CUI [3,2])
C0520666 (UMLS CUI [4])
Hamilton Anxiety Rating Scale Questionnaire
Item
ham-a score >17
boolean
C3541258 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Substance Use Disorders
Item
alcohol or substance abuse within the last 6 months
boolean
C0038586 (UMLS CUI [1])
Obsessive-Compulsive Disorder
Item
current diagnosis of obsessive-compulsive disorder
boolean
C0028768 (UMLS CUI [1])
Schizophrenia | Schizoaffective Disorder | Bipolar Mood Disorder
Item
current diagnosis of schizophrenia, schizoaffective disorder, or bipolar mood disorder
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
Antipsychotic Agents
Item
use of antipsychotic medications over the two months preceding enrollment in the study
boolean
C0040615 (UMLS CUI [1])
Antidepressive Agents Dosage altered | Mood Stabilizer Dosage altered
Item
changes in antidepressant or mood stabilizer dosing over the two months preceding enrollment in the study
boolean
C0003289 (UMLS CUI [1,1])
C0420247 (UMLS CUI [1,2])
C2917435 (UMLS CUI [2,1])
C0420247 (UMLS CUI [2,2])
Adverse reaction Risperidone | Adverse reaction Paroxetine
Item
previous adverse reaction to risperidone or paroxetine.
boolean
C0559546 (UMLS CUI [1,1])
C0073393 (UMLS CUI [1,2])
C0559546 (UMLS CUI [2,1])
C0070122 (UMLS CUI [2,2])