ID

30473

Descripción

Efficacy and Safety of SR58611A co-Administered With Escitalopram in Adults With Major Depressive Disorder; ODM derived from: https://clinicaltrials.gov/show/NCT00432614

Link

https://clinicaltrials.gov/show/NCT00432614

Palabras clave

Versiones (2)
  1. 6/6/18 6/6/18 -
  2. 6/6/18 6/6/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

6 de junio de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Major Depressive Disorder NCT00432614

Inglés

Eligibility Major Depressive Disorder NCT00432614

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
inpatients or outpatients with major depressive disorder characterized by a recurrent major depressive episode with montgomery and asberg depression rating scale (madrs) total score => 30
Descripción

Inpatients | Outpatients | Major Depressive Disorder Montgomery-Asberg Depression Rating Scale Questionnaire | Recurrent major depressive episodes

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021562
UMLS CUI [2]
C0029921
UMLS CUI [3,1]
C1269683
UMLS CUI [3,2]
C4054475
UMLS CUI [4]
C0154409
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient is at immediate risk for suicidal behavior
Descripción

At risk Suicidal behavior

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1444641
UMLS CUI [1,2]
C1760428
patient with psychotic features, catatonic features, seasonal pattern or postpartum onset
Descripción

Psychotic symptom present | Feature Catatonic | Seasonal Affective Disorder | Depression, Postpartum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0459435
UMLS CUI [2,1]
C2348519
UMLS CUI [2,2]
C0007398
UMLS CUI [3]
C0085159
UMLS CUI [4]
C0221074
patients with a current depressive episode secondary to a general medical disorder
Descripción

Depressive episode Secondary to Disease General

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0349217
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0012634
UMLS CUI [1,4]
C0205246
patients with a lifetime history or presence of bipolar disorder, psychotic disorder, panic disorder and antisocial personality disorder
Descripción

Bipolar Disorder Lifetime | Psychotic Disorders Lifetime | Panic Disorder Lifetime | Antisocial Personality Disorder Lifetime | Bipolar Disorder | Psychotic Disorders | Panic Disorder | Antisocial Personality Disorder

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005586
UMLS CUI [1,2]
C4071830
UMLS CUI [2,1]
C0033975
UMLS CUI [2,2]
C4071830
UMLS CUI [3,1]
C0030319
UMLS CUI [3,2]
C4071830
UMLS CUI [4,1]
C0003431
UMLS CUI [4,2]
C4071830
UMLS CUI [5]
C0005586
UMLS CUI [6]
C0033975
UMLS CUI [7]
C0030319
UMLS CUI [8]
C0003431
patients with severe or unstable concomitant medical conditions
Descripción

Comorbidity Severe | Comorbidity Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0443343
pregnant, breastfeeding, or likely to become pregnant during the study
Descripción

Pregnancy | Breast Feeding | Pregnancy Probably

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0032961
UMLS CUI [3,2]
C0750492
treated with escitalopram within 6 months before the study, or who have had an adverse reaction to escitalopram
Descripción

Escitalopram | Adverse reaction Escitalopram

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1099456
UMLS CUI [2,1]
C0559546
UMLS CUI [2,2]
C1099456
the investigator will evaluate whether there are other reasons why a patient may not participate.
Descripción

Other Reason Study Subject Participation Status Excluded

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3840932
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0332196
Volver a la parte superior de la página

Similar models

Eligibility Major Depressive Disorder NCT00432614

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Inpatients | Outpatients | Major Depressive Disorder Montgomery-Asberg Depression Rating Scale Questionnaire | Recurrent major depressive episodes
Item
inpatients or outpatients with major depressive disorder characterized by a recurrent major depressive episode with montgomery and asberg depression rating scale (madrs) total score => 30
boolean
C0021562 (UMLS CUI [1])
C0029921 (UMLS CUI [2])
C1269683 (UMLS CUI [3,1])
C4054475 (UMLS CUI [3,2])
C0154409 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
At risk Suicidal behavior
Item
patient is at immediate risk for suicidal behavior
boolean
C1444641 (UMLS CUI [1,1])
C1760428 (UMLS CUI [1,2])
Psychotic symptom present | Feature Catatonic | Seasonal Affective Disorder | Depression, Postpartum
Item
patient with psychotic features, catatonic features, seasonal pattern or postpartum onset
boolean
C0459435 (UMLS CUI [1])
C2348519 (UMLS CUI [2,1])
C0007398 (UMLS CUI [2,2])
C0085159 (UMLS CUI [3])
C0221074 (UMLS CUI [4])
Depressive episode Secondary to Disease General
Item
patients with a current depressive episode secondary to a general medical disorder
boolean
C0349217 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C0205246 (UMLS CUI [1,4])
Bipolar Disorder Lifetime | Psychotic Disorders Lifetime | Panic Disorder Lifetime | Antisocial Personality Disorder Lifetime | Bipolar Disorder | Psychotic Disorders | Panic Disorder | Antisocial Personality Disorder
Item
patients with a lifetime history or presence of bipolar disorder, psychotic disorder, panic disorder and antisocial personality disorder
boolean
C0005586 (UMLS CUI [1,1])
C4071830 (UMLS CUI [1,2])
C0033975 (UMLS CUI [2,1])
C4071830 (UMLS CUI [2,2])
C0030319 (UMLS CUI [3,1])
C4071830 (UMLS CUI [3,2])
C0003431 (UMLS CUI [4,1])
C4071830 (UMLS CUI [4,2])
C0005586 (UMLS CUI [5])
C0033975 (UMLS CUI [6])
C0030319 (UMLS CUI [7])
C0003431 (UMLS CUI [8])
Comorbidity Severe | Comorbidity Unstable
Item
patients with severe or unstable concomitant medical conditions
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy Probably
Item
pregnant, breastfeeding, or likely to become pregnant during the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C0750492 (UMLS CUI [3,2])
Escitalopram | Adverse reaction Escitalopram
Item
treated with escitalopram within 6 months before the study, or who have had an adverse reaction to escitalopram
boolean
C1099456 (UMLS CUI [1])
C0559546 (UMLS CUI [2,1])
C1099456 (UMLS CUI [2,2])
Other Reason Study Subject Participation Status Excluded
Item
the investigator will evaluate whether there are other reasons why a patient may not participate.
boolean
C3840932 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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