ID

30530

Descripción

Transcranial Direct Current Stimulation (tDCS) in the Treatment of Major Depressive Disorder (MDD); ODM derived from: https://clinicaltrials.gov/show/NCT01078948

Link

https://clinicaltrials.gov/show/NCT01078948

Palabras clave

Versiones (1)
  1. 12/6/18 12/6/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

12 de junio de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT01078948

Inglés

Eligibility Major Depressive Disorder NCT01078948

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
competent to consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
have a diagnosis of major depressive disorder and are currently experiencing a major depressive episode as confirmed by the scid-iv
Descripción

Major Depressive Disorder | Major depressive episode

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1269683
UMLS CUI [2]
C0024517
treatment resistant, defined as a failure to achieve a clinical response, or an inability to tolerate, at least two trials of antidepressant medication of sufficient dose for at least 6 weeks
Descripción

Unresponsive to Treatment | Clinical Response failed | Antidepressant therapy Quantity | Intolerance to Antidepressive Agents Dosage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0205269
UMLS CUI [2,1]
C4055223
UMLS CUI [2,2]
C0231175
UMLS CUI [3,1]
C1096649
UMLS CUI [3,2]
C1265611
UMLS CUI [4,1]
C1744706
UMLS CUI [4,2]
C0003289
UMLS CUI [4,3]
C0178602
aged 18 to 75.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
concomitant medications including: benzodiazepines, mood stabilizers antidepressants and anticholinergics will be allowed. since carbamazepine has been shown to interfere with the effects of anodal tdcs, potential participants taking it will not be suitable for inclusion in the trial.
Descripción

Concomitant Agent | Benzodiazepines | Mood Stabilizer | Antidepressive Agents | Anticholinergic Agents | Carbamazepine Interferes with Anodal Stimulation Transcranial Direct Current Stimulation | Carbamazepine Excluded

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2347852
UMLS CUI [2]
C0005064
UMLS CUI [3]
C2917435
UMLS CUI [4]
C0003289
UMLS CUI [5]
C0242896
UMLS CUI [6,1]
C0006949
UMLS CUI [6,2]
C0521102
UMLS CUI [6,3]
C3850022
UMLS CUI [7,1]
C0006949
UMLS CUI [7,2]
C0332196
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
dsm-iv history of substance abuse or dependence in the last 6 months
Descripción

Substance Use Disorders | Substance Dependence

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0038580
a major and/or unstable medical or neurologic illness
Descripción

Illness Major | Nervous system disorder Major | Illness Unstable | Nervous system disorder Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205164
UMLS CUI [2,1]
C0027765
UMLS CUI [2,2]
C0205164
UMLS CUI [3,1]
C0221423
UMLS CUI [3,2]
C0443343
UMLS CUI [4,1]
C0027765
UMLS CUI [4,2]
C0443343
currently taking carbamazepine
Descripción

Carbamazepine

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006949
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
history of seizures.
Descripción

Seizures

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0036572
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Similar models

Eligibility Major Depressive Disorder NCT01078948

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
competent to consent
boolean
C0021430 (UMLS CUI [1])
Major Depressive Disorder | Major depressive episode
Item
have a diagnosis of major depressive disorder and are currently experiencing a major depressive episode as confirmed by the scid-iv
boolean
C1269683 (UMLS CUI [1])
C0024517 (UMLS CUI [2])
Unresponsive to Treatment | Clinical Response failed | Antidepressant therapy Quantity | Intolerance to Antidepressive Agents Dosage
Item
treatment resistant, defined as a failure to achieve a clinical response, or an inability to tolerate, at least two trials of antidepressant medication of sufficient dose for at least 6 weeks
boolean
C0205269 (UMLS CUI [1])
C4055223 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])
C1096649 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C0003289 (UMLS CUI [4,2])
C0178602 (UMLS CUI [4,3])
Age
Item
aged 18 to 75.
boolean
C0001779 (UMLS CUI [1])
Concomitant Agent | Benzodiazepines | Mood Stabilizer | Antidepressive Agents | Anticholinergic Agents | Carbamazepine Interferes with Anodal Stimulation Transcranial Direct Current Stimulation | Carbamazepine Excluded
Item
concomitant medications including: benzodiazepines, mood stabilizers antidepressants and anticholinergics will be allowed. since carbamazepine has been shown to interfere with the effects of anodal tdcs, potential participants taking it will not be suitable for inclusion in the trial.
boolean
C2347852 (UMLS CUI [1])
C0005064 (UMLS CUI [2])
C2917435 (UMLS CUI [3])
C0003289 (UMLS CUI [4])
C0242896 (UMLS CUI [5])
C0006949 (UMLS CUI [6,1])
C0521102 (UMLS CUI [6,2])
C3850022 (UMLS CUI [6,3])
C0006949 (UMLS CUI [7,1])
C0332196 (UMLS CUI [7,2])
Item Group
C0680251 (UMLS CUI)
Substance Use Disorders | Substance Dependence
Item
dsm-iv history of substance abuse or dependence in the last 6 months
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
Illness Major | Nervous system disorder Major | Illness Unstable | Nervous system disorder Unstable
Item
a major and/or unstable medical or neurologic illness
boolean
C0221423 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0027765 (UMLS CUI [2,1])
C0205164 (UMLS CUI [2,2])
C0221423 (UMLS CUI [3,1])
C0443343 (UMLS CUI [3,2])
C0027765 (UMLS CUI [4,1])
C0443343 (UMLS CUI [4,2])
Carbamazepine
Item
currently taking carbamazepine
boolean
C0006949 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Seizures
Item
history of seizures.
boolean
C0036572 (UMLS CUI [1])
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