ID

19453

Descrizione

Risperidone vs. Bupropion ER Augmentation of SSRIs in Treatment-Resistant Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00179244

collegamento

https://clinicaltrials.gov/show/NCT00179244

Keywords

versioni (1)
  1. 03/01/17 03/01/17 -
Caricato su

3 gennaio 2017

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Unipolar Depression NCT00179244

Inglese

Eligibility Unipolar Depression NCT00179244

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female 18 years or older
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
dsm-iv diagnosis of major depressive disorder of at least moderate severity, but without psychotic features
Descrizione

DEPRESSIVE DISORDER MAJOR WITHOUT PSYCHOTIC FEATURE Moderate | Severe major depression without psychotic features

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0743081
UMLS CUI [1,2]
C0205081
UMLS CUI [2]
C0270457
ham-d 17 score of 18 or above
Descrizione

Hamilton rating scale for depression

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0451203
have a documentable history of 2 prior adequate trials of antidepressants including an ssri without sufficient response. a clinically adequate trial is defined as having taken a minimum effective dose of an antidepressant for at least 3 weeks without a significant change in depressive symptoms.
Descrizione

Antidepressive Agents Trials Quantity | Selective Serotonin Reuptake Inhibitors | Depressive Symptoms Absent response to treatment

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1265611
UMLS CUI [2]
C0360105
UMLS CUI [3,1]
C0086132
UMLS CUI [3,2]
C0438286
must be currently on an serotonin uptake inhibitor (to include venlafaxine or duloxetine) at an adequate dose for at least 3 weeks.
Descrizione

Serotonin Uptake Inhibitor Dose Adequate | venlafaxine | duloxetine

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0162758
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205411
UMLS CUI [2]
C0078569
UMLS CUI [3]
C0245561
ability and willingness to provide consent for participation in the study.
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
any medical condition that would preclude treatment with an ssri, risperidone, or bupropion er
Descrizione

Medical condition Excludes Selective Serotonin Reuptake Inhibitors | Medical condition Excludes Risperidone | Medical condition Excludes Bupropion Extended Release

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0360105
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C0073393
UMLS CUI [3,1]
C3843040
UMLS CUI [3,2]
C0332196
UMLS CUI [3,3]
C1252646
any clinically significant unstable medical condition
Descrizione

Medical condition Unstable Clinical Significance

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0443343
UMLS CUI [1,3]
C2826293
diagnosis of bipolar disorder or a primary diagnosis of any psychotic disorder
Descrizione

Bipolar Disorder | Psychotic Disorder Primary

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0005586
UMLS CUI [2,1]
C0033975
UMLS CUI [2,2]
C0205225
current psychotic symptoms (hallucination or delusions)
Descrizione

Psychotic symptom | Hallucinations | Delusions

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0871189
UMLS CUI [2]
C0018524
UMLS CUI [3]
C0011253
alcohol or drug abuse or dependence in the last 3 months (excluding nicotine and caffeine dependence/abuse) or abuse within the last month
Descrizione

Substance Use Disorders | Substance Dependence | Nicotine Dependence | Nicotine abuse | Caffeine dependence | Caffeine abuse

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0038580
UMLS CUI [3]
C0028043
UMLS CUI [4]
C2363943
UMLS CUI [5]
C1386553
UMLS CUI [6]
C0679260
documented non-response to the combination of a novel antipsychotic or bupropion er and a ssri
Descrizione

Antipsychotic Agent New | Bupropion Extended Release | Selective Serotonin Reuptake Inhibitors | Absent response to treatment

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0040615
UMLS CUI [1,2]
C0205314
UMLS CUI [2]
C1252646
UMLS CUI [3]
C0360105
UMLS CUI [4]
C0438286
concomitant use of any psychotropic other than an ssri or zolpidem (prn for sleep)
Descrizione

Psychotropic Drugs | Selective Serotonin Reuptake Inhibitors | zolpidem

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0033978
UMLS CUI [2]
C0360105
UMLS CUI [3]
C0078839
score of 4 on the suicide item of the ham-d scale and determination by the investigator of significant suicide risk
Descrizione

Hamilton rating scale for depression | At risk for suicide Significant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0451203
UMLS CUI [2,1]
C0563664
UMLS CUI [2,2]
C0750502
known sensitivity to risperidone or bupropion er
Descrizione

Hypersensitivity Risperidone | Hypersensitivity Bupropion Extended Release

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0073393
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1252646
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Similar models

Eligibility Unipolar Depression NCT00179244

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female 18 years or older
boolean
C0001779 (UMLS CUI [1])
DEPRESSIVE DISORDER MAJOR WITHOUT PSYCHOTIC FEATURE Moderate | Severe major depression without psychotic features
Item
dsm-iv diagnosis of major depressive disorder of at least moderate severity, but without psychotic features
boolean
C0743081 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0270457 (UMLS CUI [2])
Hamilton rating scale for depression
Item
ham-d 17 score of 18 or above
boolean
C0451203 (UMLS CUI [1])
Antidepressive Agents Trials Quantity | Selective Serotonin Reuptake Inhibitors | Depressive Symptoms Absent response to treatment
Item
have a documentable history of 2 prior adequate trials of antidepressants including an ssri without sufficient response. a clinically adequate trial is defined as having taken a minimum effective dose of an antidepressant for at least 3 weeks without a significant change in depressive symptoms.
boolean
C0003289 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0360105 (UMLS CUI [2])
C0086132 (UMLS CUI [3,1])
C0438286 (UMLS CUI [3,2])
Serotonin Uptake Inhibitor Dose Adequate | venlafaxine | duloxetine
Item
must be currently on an serotonin uptake inhibitor (to include venlafaxine or duloxetine) at an adequate dose for at least 3 weeks.
boolean
C0162758 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205411 (UMLS CUI [1,3])
C0078569 (UMLS CUI [2])
C0245561 (UMLS CUI [3])
Informed Consent
Item
ability and willingness to provide consent for participation in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical condition Excludes Selective Serotonin Reuptake Inhibitors | Medical condition Excludes Risperidone | Medical condition Excludes Bupropion Extended Release
Item
any medical condition that would preclude treatment with an ssri, risperidone, or bupropion er
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0360105 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0073393 (UMLS CUI [2,3])
C3843040 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C1252646 (UMLS CUI [3,3])
Medical condition Unstable Clinical Significance
Item
any clinically significant unstable medical condition
boolean
C3843040 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,3])
Bipolar Disorder | Psychotic Disorder Primary
Item
diagnosis of bipolar disorder or a primary diagnosis of any psychotic disorder
boolean
C0005586 (UMLS CUI [1])
C0033975 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
Psychotic symptom | Hallucinations | Delusions
Item
current psychotic symptoms (hallucination or delusions)
boolean
C0871189 (UMLS CUI [1])
C0018524 (UMLS CUI [2])
C0011253 (UMLS CUI [3])
Substance Use Disorders | Substance Dependence | Nicotine Dependence | Nicotine abuse | Caffeine dependence | Caffeine abuse
Item
alcohol or drug abuse or dependence in the last 3 months (excluding nicotine and caffeine dependence/abuse) or abuse within the last month
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
C0028043 (UMLS CUI [3])
C2363943 (UMLS CUI [4])
C1386553 (UMLS CUI [5])
C0679260 (UMLS CUI [6])
Antipsychotic Agent New | Bupropion Extended Release | Selective Serotonin Reuptake Inhibitors | Absent response to treatment
Item
documented non-response to the combination of a novel antipsychotic or bupropion er and a ssri
boolean
C0040615 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C1252646 (UMLS CUI [2])
C0360105 (UMLS CUI [3])
C0438286 (UMLS CUI [4])
Psychotropic Drugs | Selective Serotonin Reuptake Inhibitors | zolpidem
Item
concomitant use of any psychotropic other than an ssri or zolpidem (prn for sleep)
boolean
C0033978 (UMLS CUI [1])
C0360105 (UMLS CUI [2])
C0078839 (UMLS CUI [3])
Hamilton rating scale for depression | At risk for suicide Significant
Item
score of 4 on the suicide item of the ham-d scale and determination by the investigator of significant suicide risk
boolean
C0451203 (UMLS CUI [1])
C0563664 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
Hypersensitivity Risperidone | Hypersensitivity Bupropion Extended Release
Item
known sensitivity to risperidone or bupropion er
boolean
C0020517 (UMLS CUI [1,1])
C0073393 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1252646 (UMLS CUI [2,2])
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