ID

30502

Description

Antidepressant Incomplete Response Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00782964

Lien

https://clinicaltrials.gov/show/NCT00782964

Mots-clés

Versions (1)
  1. 09/06/2018 09/06/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

9 juin 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT00782964

Anglais

Eligibility Major Depressive Disorder NCT00782964

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
provision of written inform consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
diagnosed of major depressive disorder based on dsm-iv-tr
Description

Major Depressive Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C1269683
outpatient who has a change in pharmacological therapeutic plan after an incomplete response or intolerance to a treatment with an adequate dosage of an antidepressant (ssri/nsri) 5
Description

Outpatients | Pharmacotherapy Plan Change | Status post Partial response | Intolerance to Antidepressive Agents Dosage | Intolerance to Selective Serotonin Reuptake Inhibitors | Intolerance to Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs)

Type de données

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C1301732
UMLS CUI [2,3]
C0443172
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C1521726
UMLS CUI [4,1]
C1744706
UMLS CUI [4,2]
C0003289
UMLS CUI [4,3]
C0178602
UMLS CUI [5,1]
C1744706
UMLS CUI [5,2]
C0360105
UMLS CUI [6,1]
C1744706
UMLS CUI [6,2]
C1579361
able to understand and to comply with requirements of the study
Description

Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
mental retardation
Description

Mental Retardation

Type de données

boolean

Alias
UMLS CUI [1]
C0025362
to have been recruited in a clinical trial in the last 4 weeks or to have planned the inclusion in a clinical trial during the follow-up of this study
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
mdd secondary to substance abuse or somatic illness
Description

Major Depressive Disorder Secondary to Substance Use Disorders | Major Depressive Disorder Secondary to Illness Somatic

Type de données

boolean

Alias
UMLS CUI [1,1]
C1269683
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0038586
UMLS CUI [2,1]
C1269683
UMLS CUI [2,2]
C0175668
UMLS CUI [2,3]
C0221423
UMLS CUI [2,4]
C2986476
actual depressive episode with <4 weeks or >12 months of length
Description

Depressive episode Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0349217
UMLS CUI [1,2]
C0449238
current treatment with >1 ssri/srni or previous treatment with >1 ssri/srni, augmentation treatment with ssri/srni, intravenous antidepressant treatment, tms, ect or mao
Description

Selective Serotonin Reuptake Inhibitors Quantity | Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) Quantity | Selective Serotonin Reuptake Inhibitors augmented | Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) augmented | Antidepressive Agents Intravenous | Transcranial magnetic stimulation | Electroconvulsive Therapy | Monoamine Oxidase Inhibitors

Type de données

boolean

Alias
UMLS CUI [1,1]
C0360105
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C1579361
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0360105
UMLS CUI [3,2]
C0205217
UMLS CUI [4,1]
C1579361
UMLS CUI [4,2]
C0205217
UMLS CUI [5,1]
C0003289
UMLS CUI [5,2]
C1522726
UMLS CUI [6]
C0436548
UMLS CUI [7]
C0013806
UMLS CUI [8]
C0026457
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Similar models

Eligibility Major Depressive Disorder NCT00782964

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
provision of written inform consent
boolean
C0021430 (UMLS CUI [1])
Major Depressive Disorder
Item
diagnosed of major depressive disorder based on dsm-iv-tr
boolean
C1269683 (UMLS CUI [1])
Outpatients | Pharmacotherapy Plan Change | Status post Partial response | Intolerance to Antidepressive Agents Dosage | Intolerance to Selective Serotonin Reuptake Inhibitors | Intolerance to Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs)
Item
outpatient who has a change in pharmacological therapeutic plan after an incomplete response or intolerance to a treatment with an adequate dosage of an antidepressant (ssri/nsri) 5
boolean
C0029921 (UMLS CUI [1])
C0013216 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0443172 (UMLS CUI [2,3])
C0231290 (UMLS CUI [3,1])
C1521726 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C0003289 (UMLS CUI [4,2])
C0178602 (UMLS CUI [4,3])
C1744706 (UMLS CUI [5,1])
C0360105 (UMLS CUI [5,2])
C1744706 (UMLS CUI [6,1])
C1579361 (UMLS CUI [6,2])
Protocol Compliance
Item
able to understand and to comply with requirements of the study
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Mental Retardation
Item
mental retardation
boolean
C0025362 (UMLS CUI [1])
Study Subject Participation Status
Item
to have been recruited in a clinical trial in the last 4 weeks or to have planned the inclusion in a clinical trial during the follow-up of this study
boolean
C2348568 (UMLS CUI [1])
Major Depressive Disorder Secondary to Substance Use Disorders | Major Depressive Disorder Secondary to Illness Somatic
Item
mdd secondary to substance abuse or somatic illness
boolean
C1269683 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0038586 (UMLS CUI [1,3])
C1269683 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0221423 (UMLS CUI [2,3])
C2986476 (UMLS CUI [2,4])
Depressive episode Duration
Item
actual depressive episode with <4 weeks or >12 months of length
boolean
C0349217 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Selective Serotonin Reuptake Inhibitors Quantity | Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) Quantity | Selective Serotonin Reuptake Inhibitors augmented | Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) augmented | Antidepressive Agents Intravenous | Transcranial magnetic stimulation | Electroconvulsive Therapy | Monoamine Oxidase Inhibitors
Item
current treatment with >1 ssri/srni or previous treatment with >1 ssri/srni, augmentation treatment with ssri/srni, intravenous antidepressant treatment, tms, ect or mao
boolean
C0360105 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1579361 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0360105 (UMLS CUI [3,1])
C0205217 (UMLS CUI [3,2])
C1579361 (UMLS CUI [4,1])
C0205217 (UMLS CUI [4,2])
C0003289 (UMLS CUI [5,1])
C1522726 (UMLS CUI [5,2])
C0436548 (UMLS CUI [6])
C0013806 (UMLS CUI [7])
C0026457 (UMLS CUI [8])
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