ID

30511

Description

N-methylglycine (Sarcosine) Treatment for Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00977353

Link

https://clinicaltrials.gov/show/NCT00977353

Keywords

Versions (1)
  1. 6/10/18 6/10/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 10, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Major Depressive Disorder NCT00977353

English

Eligibility Major Depressive Disorder NCT00977353

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18-55 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
fulfilled the dsm-iv criteria of major depressive disorder
Description

Major Depressive Disorder

Data type

boolean

Alias
UMLS CUI [1]
C1269683
had a 17-item hamilton rating scale for depression (hamd-17)>or= 18
Description

Hamilton Depression Rating Scale 17 Item Clinical Classification

Data type

boolean

Alias
UMLS CUI [1]
C3639712
no dsm-iv diagnosis of substance abuse or dependence (including alcohol) within the past 6 months
Description

Substance Use Disorders Absent | Substance Dependence Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0038580
UMLS CUI [2,2]
C0332197
had been drug free for > 3 months
Description

Drugs Free of

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0332296
physically healthy and had all laboratory parameters within normal limits.
Description

Healthy Physical | Laboratory Results Within Normal Limits

Data type

boolean

Alias
UMLS CUI [1,1]
C3898900
UMLS CUI [1,2]
C0205485
UMLS CUI [2,1]
C1254595
UMLS CUI [2,2]
C0442816
agree to participate in the study and provide informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
had history of epilepsy, head trauma or other major neurological or medical diseases
Description

Epilepsy | Craniocerebral Trauma | Nervous system disorde Major | Disease Major

Data type

boolean

Alias
UMLS CUI [1]
C0014544
UMLS CUI [2]
C0018674
UMLS CUI [3,1]
C0027765
UMLS CUI [3,2]
C0205164
UMLS CUI [4,1]
C0012634
UMLS CUI [4,2]
C0205164
had psychotic depression, bipolar i/ii disorder, schizophrenia or any other psychotic disorder
Description

Depression, psychotic | Bipolar I disorder | Bipolar II disorder | Schizophrenia | Psychotic Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0743072
UMLS CUI [2]
C0853193
UMLS CUI [3]
C0236788
UMLS CUI [4]
C0036341
UMLS CUI [5]
C0033975
moderate-severe suicidal risks
Description

Moderate suicide risk | At risk for suicide Severe

Data type

boolean

Alias
UMLS CUI [1]
C1271075
UMLS CUI [2,1]
C0563664
UMLS CUI [2,2]
C0205082
severe cognitive impairment
Description

Severe cognitive impairment

Data type

boolean

Alias
UMLS CUI [1]
C3554639
female subjects who were pregnant, or at risk of pregnancy or lactation
Description

Pregnancy | At risk Pregnancy | At risk Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C1444641
UMLS CUI [2,2]
C0032961
UMLS CUI [3,1]
C1444641
UMLS CUI [3,2]
C0006147
initiating or stopping formal psychotherapy within six weeks prior to enrollment
Description

Psychotherapy Initiation | Psychotherapy Discontinuation

Data type

boolean

Alias
UMLS CUI [1,1]
C0033968
UMLS CUI [1,2]
C1704686
UMLS CUI [2,1]
C0033968
UMLS CUI [2,2]
C1444662
had a history of poor response to ssris or previously received electroconvulsive therapy
Description

Poor response to Selective Serotonin Reuptake Inhibitors | Electroconvulsive Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1320680
UMLS CUI [1,2]
C0360105
UMLS CUI [2]
C0013806
had a history of severe adverse reaction to ssris.
Description

Adverse reaction Severe Selective Serotonin Reuptake Inhibitors

Data type

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0360105
Back to the top of the page

Similar models

Eligibility Major Depressive Disorder NCT00977353

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 18-55 years
boolean
C0001779 (UMLS CUI [1])
Major Depressive Disorder
Item
fulfilled the dsm-iv criteria of major depressive disorder
boolean
C1269683 (UMLS CUI [1])
Hamilton Depression Rating Scale 17 Item Clinical Classification
Item
had a 17-item hamilton rating scale for depression (hamd-17)>or= 18
boolean
C3639712 (UMLS CUI [1])
Substance Use Disorders Absent | Substance Dependence Absent
Item
no dsm-iv diagnosis of substance abuse or dependence (including alcohol) within the past 6 months
boolean
C0038586 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Drugs Free of
Item
had been drug free for > 3 months
boolean
C0013227 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
Healthy Physical | Laboratory Results Within Normal Limits
Item
physically healthy and had all laboratory parameters within normal limits.
boolean
C3898900 (UMLS CUI [1,1])
C0205485 (UMLS CUI [1,2])
C1254595 (UMLS CUI [2,1])
C0442816 (UMLS CUI [2,2])
Informed Consent
Item
agree to participate in the study and provide informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Epilepsy | Craniocerebral Trauma | Nervous system disorde Major | Disease Major
Item
had history of epilepsy, head trauma or other major neurological or medical diseases
boolean
C0014544 (UMLS CUI [1])
C0018674 (UMLS CUI [2])
C0027765 (UMLS CUI [3,1])
C0205164 (UMLS CUI [3,2])
C0012634 (UMLS CUI [4,1])
C0205164 (UMLS CUI [4,2])
Depression, psychotic | Bipolar I disorder | Bipolar II disorder | Schizophrenia | Psychotic Disorders
Item
had psychotic depression, bipolar i/ii disorder, schizophrenia or any other psychotic disorder
boolean
C0743072 (UMLS CUI [1])
C0853193 (UMLS CUI [2])
C0236788 (UMLS CUI [3])
C0036341 (UMLS CUI [4])
C0033975 (UMLS CUI [5])
Moderate suicide risk | At risk for suicide Severe
Item
moderate-severe suicidal risks
boolean
C1271075 (UMLS CUI [1])
C0563664 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Severe cognitive impairment
Item
severe cognitive impairment
boolean
C3554639 (UMLS CUI [1])
Pregnancy | At risk Pregnancy | At risk Breast Feeding
Item
female subjects who were pregnant, or at risk of pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C1444641 (UMLS CUI [2,1])
C0032961 (UMLS CUI [2,2])
C1444641 (UMLS CUI [3,1])
C0006147 (UMLS CUI [3,2])
Psychotherapy Initiation | Psychotherapy Discontinuation
Item
initiating or stopping formal psychotherapy within six weeks prior to enrollment
boolean
C0033968 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
C0033968 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
Poor response to Selective Serotonin Reuptake Inhibitors | Electroconvulsive Therapy
Item
had a history of poor response to ssris or previously received electroconvulsive therapy
boolean
C1320680 (UMLS CUI [1,1])
C0360105 (UMLS CUI [1,2])
C0013806 (UMLS CUI [2])
Adverse reaction Severe Selective Serotonin Reuptake Inhibitors
Item
had a history of severe adverse reaction to ssris.
boolean
C0559546 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0360105 (UMLS CUI [1,3])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial