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Informations:
Erreur:
ID
30472
Description
Efficacy and Safety of SR58611A co-Administered With Escitalopram in Adults With Major Depressive Disorder; ODM derived from: https://clinicaltrials.gov/show/NCT00432614
Lien
https://clinicaltrials.gov/show/NCT00432614
Mots-clés
Versions (2)
- 06/06/2018 06/06/2018 -
- 06/06/2018 06/06/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
6 juin 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Eligibility Major Depressive Disorder NCT00432614
Eligibility Major Depressive Disorder NCT00432614
- StudyEvent: Eligibility
Similar models
Eligibility Major Depressive Disorder NCT00432614
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Inpatients | Outpatients | Major Depressive Disorder | Recurrent major depressive episodes Montgomery-Asberg Depression Rating Scale Questionnaire
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])
C0154409 (UMLS CUI [4,1])
C4054475 (UMLS CUI [4,2])
C0029921 (UMLS CUI [2])
C1269683 (UMLS CUI [3])
C0154409 (UMLS CUI [4,1])
C4054475 (UMLS CUI [4,2])
At risk Suicidal behavior
Item
patient is at immediate risk for suicidal behavior
boolean
C1444641 (UMLS CUI [1,1])
C1760428 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])