ID

16473

Description

Study Of The Effects Of A New Antidepressant Therapy In Patients With Major Depressive Disorder (MDD); ODM derived from: https://clinicaltrials.gov/show/NCT00413023

Link

https://clinicaltrials.gov/show/NCT00413023

Keywords

  1. 7/17/16 7/17/16 -
Uploaded on

July 17, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Depressive Disorder, Major NCT00413023

Eligibility Depressive Disorder, Major NCT00413023

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
primary diagnosis of major depressive disorder as defined in dsm-iv.
Description

Major depressive disorder DSM-IV

Data type

boolean

Alias
UMLS CUI [1,1]
C1269683
UMLS CUI [1,2]
C0220952
capable of giving informed consent and willing to comply with the study requirements.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
women of childbearing potential must agree to one of a number of defined acceptable methods of birth control.
Description

Contraception

Data type

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
primary diagnosis within the past 6 months of another axis 1 disorder such as an anxiety disorder.
Description

Axis I diagnosis

Data type

boolean

Alias
UMLS CUI [1]
C0270287
use of medications for a psychiatric condition including herbals in the past 2-12 weeks according to medication type.
Description

use of medications for a psychiatric condition

Data type

boolean

Alias
UMLS CUI [1]
C0013227
subjects who, in the investigator's judgement, pose a current, serious suicidal or homicidal risk or have made a suicide attempt within the past 6 months.
Description

Suicidal or homicidal risk

Data type

boolean

Alias
UMLS CUI [1]
C0438696
UMLS CUI [2]
C0745031
subjects who currently meet or who met within 6 months prior to screening dsm-iv criteria for substance abuse or subjects who currently meet or who met within 6 months prior to screening dsm-iv criteria for substance dependence (other than nicotine).
Description

Substance abuse

Data type

boolean

Alias
UMLS CUI [1]
C0038586
significantly abnormal blood or urine laboratory tests or electrocardiogram (ecg).
Description

abnormal blood or urine laboratory tests or electrocardiogram

Data type

boolean

Alias
UMLS CUI [1]
C0022885
UMLS CUI [2]
C1623258

Similar models

Eligibility Depressive Disorder, Major NCT00413023

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Major depressive disorder DSM-IV
Item
primary diagnosis of major depressive disorder as defined in dsm-iv.
boolean
C1269683 (UMLS CUI [1,1])
C0220952 (UMLS CUI [1,2])
informed consent
Item
capable of giving informed consent and willing to comply with the study requirements.
boolean
C0021430 (UMLS CUI [1])
Contraception
Item
women of childbearing potential must agree to one of a number of defined acceptable methods of birth control.
boolean
C0700589 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Axis I diagnosis
Item
primary diagnosis within the past 6 months of another axis 1 disorder such as an anxiety disorder.
boolean
C0270287 (UMLS CUI [1])
use of medications for a psychiatric condition
Item
use of medications for a psychiatric condition including herbals in the past 2-12 weeks according to medication type.
boolean
C0013227 (UMLS CUI [1])
Suicidal or homicidal risk
Item
subjects who, in the investigator's judgement, pose a current, serious suicidal or homicidal risk or have made a suicide attempt within the past 6 months.
boolean
C0438696 (UMLS CUI [1])
C0745031 (UMLS CUI [2])
Substance abuse
Item
subjects who currently meet or who met within 6 months prior to screening dsm-iv criteria for substance abuse or subjects who currently meet or who met within 6 months prior to screening dsm-iv criteria for substance dependence (other than nicotine).
boolean
C0038586 (UMLS CUI [1])
abnormal blood or urine laboratory tests or electrocardiogram
Item
significantly abnormal blood or urine laboratory tests or electrocardiogram (ecg).
boolean
C0022885 (UMLS CUI [1])
C1623258 (UMLS CUI [2])

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