Informatie:
Fout:
ID
28883
Beschrijving
Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00837486
Link
https://clinicaltrials.gov/show/NCT00837486
Trefwoorden
Versies (1)
- 10-02-18 10-02-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
10 februari 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Depression NCT00837486
Eligibility Depression NCT00837486
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT00837486
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Protocol Compliance | Informed Consent
Item
consent to participate in screening and study procedures by signing and dating the informed consent form
boolean
C0525058 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
Major Depressive Disorder
Item
are diagnosed with major depressive disorder (mdd)
boolean
C1269683 (UMLS CUI [1])
Therapeutic procedure Different Quantity | Antidepressive Agents | Combined Modality Therapy | Electroconvulsive Therapy
Item
have tried at least 4 different treatments, for example antidepressant medications, combinations of antidepressant medications, and/or electroconvulsive therapy (ect)
boolean
C0087111 (UMLS CUI [1,1])
C1705242 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0003289 (UMLS CUI [2])
C0009429 (UMLS CUI [3])
C0013806 (UMLS CUI [4])
C1705242 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0003289 (UMLS CUI [2])
C0009429 (UMLS CUI [3])
C0013806 (UMLS CUI [4])
Montgomery-Asberg Depression Rating Scale Questionnaire
Item
screening madrs score ≥ 28
boolean
C4054475 (UMLS CUI [1])
Major depressive episode persistent Duration
Item
have had the current major depressive episode persist for at least 2 years
boolean
C0024517 (UMLS CUI [1,1])
C0205322 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0205322 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Childbearing Potential Contraceptive methods
Item
females, if of child-bearing potential, must be using an acceptable method of birth control
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Pregnancy
Item
females: currently pregnant
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status Interferes with Research results | Investigational New Drugs | Investigational Medical Device
Item
currently enrolled in or plan to enroll in any concurrent drug and/or device study that may confound the results of this study
boolean
C2348568 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Nervous system disorder compromises Clinical Trial Safety | Nervous system disorder compromises Clinical Trial Completion
Item
have a neurological condition that may jeopardize the safety or the conduct of the study
boolean
C0027765 (UMLS CUI [1,1])
C2945640 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0036043 (UMLS CUI [1,4])
C0027765 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C0205197 (UMLS CUI [2,4])
C2945640 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0036043 (UMLS CUI [1,4])
C0027765 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C0205197 (UMLS CUI [2,4])
Medical condition Inappropriate Deep Brain Stimulation
Item
have any medical conditions unsuitable for undergoing dbs surgery
boolean
C3843040 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0394162 (UMLS CUI [1,3])
C1548788 (UMLS CUI [1,2])
C0394162 (UMLS CUI [1,3])