ID

21818

Description

Efficacy, Safety and Tolerability of Agomelatine in the Treatment of Major Depressive Disorder; ODM derived from: https://clinicaltrials.gov/show/NCT00411242

Link

https://clinicaltrials.gov/show/NCT00411242

Keywords

  1. 4/30/17 4/30/17 -
  2. 5/2/17 5/2/17 -
Uploaded on

May 2, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Major Depressive Disorder (MDD) NCT00411242

Eligibility Major Depressive Disorder (MDD) NCT00411242

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of major depressive disorder, single or recurrent episode, according to dsm-iv criteria
Description

Single major depressive episode | Recurrent major depressive episodes

Data type

boolean

Alias
UMLS CUI [1]
C0024517
UMLS CUI [2]
C0154409
ham-d17 total score > or = 22 at screening and baseline
Description

Hamilton Depression Rating Scale 17 Item Questionnaire

Data type

boolean

Alias
UMLS CUI [1]
C3639712
cgi-severity score > or = 4 at screening and baseline
Description

Clinical Global Impression Questionnaire

Data type

boolean

Alias
UMLS CUI [1]
C3639708
only patients who complete the core protocol are eligible to participate in the open-label extension phase
Description

Protocol Compliance Complete | Participation Open Label Study

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C1709323
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of bipolar disorder (i or ii), schizophrenia, schizoaffective disorder, eating disorder, or obsessive compulsive disorder
Description

Bipolar I disorder | Bipolar II disorder | Schizophrenia | Schizoaffective Disorder | Eating Disorders | Obsessive-Compulsive Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0853193
UMLS CUI [2]
C0236788
UMLS CUI [3]
C0036341
UMLS CUI [4]
C0036337
UMLS CUI [5]
C0013473
UMLS CUI [6]
C0028768
any current axis i disorder other than major depressive disorder which is the focus of treatment
Description

Axis I diagnosis | Major Depressive Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0270287
UMLS CUI [2]
C1269683
substance or alcohol abuse in the last 30 days, dependence in the last 6 months
Description

Substance Use Disorders | Substance Dependence

Data type

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0038580
concomitant psychotropic medication, including herbal preparations and melatonin
Description

Psychotropic Drugs | Plant Preparations | Melatonin

Data type

boolean

Alias
UMLS CUI [1]
C0033978
UMLS CUI [2]
C0949854
UMLS CUI [3]
C0025219
psychotherapy of any type
Description

Psychotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0033968
female patients of childbearing potential who are not using effective contraception
Description

Childbearing Potential Contraceptive methods Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332268
other protocol-defined inclusion/exclusion criteria may apply
Description

Clinical Trial Eligibility Criteria Study Protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563

Similar models

Eligibility Major Depressive Disorder (MDD) NCT00411242

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Single major depressive episode | Recurrent major depressive episodes
Item
diagnosis of major depressive disorder, single or recurrent episode, according to dsm-iv criteria
boolean
C0024517 (UMLS CUI [1])
C0154409 (UMLS CUI [2])
Hamilton Depression Rating Scale 17 Item Questionnaire
Item
ham-d17 total score > or = 22 at screening and baseline
boolean
C3639712 (UMLS CUI [1])
Clinical Global Impression Questionnaire
Item
cgi-severity score > or = 4 at screening and baseline
boolean
C3639708 (UMLS CUI [1])
Protocol Compliance Complete | Participation Open Label Study
Item
only patients who complete the core protocol are eligible to participate in the open-label extension phase
boolean
C0525058 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0679823 (UMLS CUI [2,1])
C1709323 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Bipolar I disorder | Bipolar II disorder | Schizophrenia | Schizoaffective Disorder | Eating Disorders | Obsessive-Compulsive Disorder
Item
history of bipolar disorder (i or ii), schizophrenia, schizoaffective disorder, eating disorder, or obsessive compulsive disorder
boolean
C0853193 (UMLS CUI [1])
C0236788 (UMLS CUI [2])
C0036341 (UMLS CUI [3])
C0036337 (UMLS CUI [4])
C0013473 (UMLS CUI [5])
C0028768 (UMLS CUI [6])
Axis I diagnosis | Major Depressive Disorder
Item
any current axis i disorder other than major depressive disorder which is the focus of treatment
boolean
C0270287 (UMLS CUI [1])
C1269683 (UMLS CUI [2])
Substance Use Disorders | Substance Dependence
Item
substance or alcohol abuse in the last 30 days, dependence in the last 6 months
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
Psychotropic Drugs | Plant Preparations | Melatonin
Item
concomitant psychotropic medication, including herbal preparations and melatonin
boolean
C0033978 (UMLS CUI [1])
C0949854 (UMLS CUI [2])
C0025219 (UMLS CUI [3])
Psychotherapy
Item
psychotherapy of any type
boolean
C0033968 (UMLS CUI [1])
Childbearing Potential Contraceptive methods Lacking
Item
female patients of childbearing potential who are not using effective contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Clinical Trial Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])

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