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ID
33890
Beschrijving
A Study Of The Efficacy And Safety Of CP-601,927 Augmentation Of Antidepressant Therapy In Major Depression; ODM derived from: https://clinicaltrials.gov/show/NCT01098240
Link
https://clinicaltrials.gov/show/NCT01098240
Trefwoorden
Versies (1)
- 05-01-19 05-01-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
5 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT01098240
Eligibility Major Depressive Disorder NCT01098240
- StudyEvent: Eligibility
Similar models
Eligibility Major Depressive Disorder NCT01098240
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Healthy | Age
Item
medically healthy males or females aged 18-65 (inclusive).
boolean
C3898900 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
DEPRESSIVE DISORDER MAJOR WITHOUT PSYCHOTIC FEATURE Primary
Item
patients must have a primary current diagnosis of mdd without psychotic features.
boolean
C0743081 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,2])
Antidepressant therapy | Major depressive episode Duration | Response to treatment Adequate Absent
Item
patients must be receiving ongoing antidepressant therapy at the time of screening. duration of the current episode of mdd must be at least 8 weeks prior to enrollment without adequate response to treatment.
boolean
C1096649 (UMLS CUI [1])
C0024517 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0521982 (UMLS CUI [3,1])
C0205411 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0024517 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0521982 (UMLS CUI [3,1])
C0205411 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Mental disorders Other
Item
patients with other psychiatric disorders.
boolean
C0004936 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
Tobacco use
Item
patients who use tobacco products.
boolean
C0543414 (UMLS CUI [1])
Substance Use Disorders | Substance Dependence
Item
alcohol or substance abuse or dependence.
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
C0038580 (UMLS CUI [2])
Monoamine Oxidase Inhibitors
Item
treatment with a monoamine oxidase inhibitor within 10 weeks of enrollment.
boolean
C0026457 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Laboratory test result abnormal | Electrocardiogram abnormal | Physical examination abnormal | Neurological examination abnormal
Item
clinically significant abnormalities on laboratory tests, electrocardiogram, or physical or neurologic examination.
boolean
C0438215 (UMLS CUI [1])
C0522055 (UMLS CUI [2])
C0747585 (UMLS CUI [3])
C1112537 (UMLS CUI [4])
C0522055 (UMLS CUI [2])
C0747585 (UMLS CUI [3])
C1112537 (UMLS CUI [4])