ID

30511

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00977353

Trefwoorden

Versies (1)
  1. 10-06-18 10-06-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

10 juni 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Major Depressive Disorder NCT00977353

Engels

Eligibility Major Depressive Disorder NCT00977353

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18-55 years
Beschrijving

Age

Datatype

boolean

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

Major Depressive Disorder

Datatype

boolean

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

Hamilton Depression Rating Scale 17 Item Clinical Classification

Datatype

boolean

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

Substance Use Disorders Absent | Substance Dependence Absent

Datatype

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
Beschrijving

Drugs Free of

Datatype

boolean

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

Healthy Physical | Laboratory Results Within Normal Limits

Datatype

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
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

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

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Moderate suicide risk | At risk for suicide Severe

Datatype

boolean

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

Severe cognitive impairment

Datatype

boolean

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

Pregnancy | At risk Pregnancy | At risk Breast Feeding

Datatype

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
Beschrijving

Psychotherapy Initiation | Psychotherapy Discontinuation

Datatype

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
Beschrijving

Poor response to Selective Serotonin Reuptake Inhibitors | Electroconvulsive Therapy

Datatype

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.
Beschrijving

Adverse reaction Severe Selective Serotonin Reuptake Inhibitors

Datatype

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0360105
Terug naar het begin van de pagina

Similar models

Eligibility Major Depressive Disorder NCT00977353

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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