Informatie:
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ID
17100
Beschrijving
Depression Study In Elderly Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00067444
Link
https://clinicaltrials.gov/show/NCT00067444
Trefwoorden
Versies (2)
- 24-08-16 24-08-16 -
- 25-08-16 25-08-16 -
Geüploaded op
25 augustus 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Depressive Disorder, Major NCT00067444
Eligibility Depressive Disorder, Major NCT00067444
- StudyEvent: Eligibility
Similar models
Eligibility Depressive Disorder, Major NCT00067444
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Major Depressive Disorder
Item
diagnosis of major depressive disorder (mdd).
boolean
C1269683 (UMLS CUI [1])
Single major depressive episode Duration
Item
current major depressive episode at screen at least 2 months duration.
boolean
C0024517 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Age
Item
must be at least 60 years of age.
boolean
C0001779 (UMLS CUI [1])
Principal diagnosis | Major Depressive Disorder
Item
patients with a primary diagnosis other than mdd.
boolean
C0332137 (UMLS CUI [1])
C1269683 (UMLS CUI [2])
C1269683 (UMLS CUI [2])
Schizophrenia | Schizoaffective Disorder | Bipolar Disorder | Dementia
Item
patients with a history of schizophrenia, schizoaffective disorder, bipolar disorder or dementia.
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
C0497327 (UMLS CUI [4])
C0036337 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
C0497327 (UMLS CUI [4])
Duration Depressive episode Brief
Item
patients with a history of brief depressive episodes lasting less than 8 weeks.
boolean
C0449238 (UMLS CUI [1,1])
C0349217 (UMLS CUI [1,2])
C1879313 (UMLS CUI [1,3])
C0349217 (UMLS CUI [1,2])
C1879313 (UMLS CUI [1,3])
Formal psychological therapy
Item
patients receiving formal psychotherapy within 12 weeks of study.
boolean
C1320526 (UMLS CUI [1])
Suicidal
Item
patients who are suicidal.
boolean
C0438696 (UMLS CUI [1])
Electroconvulsive Therapy | Transcranial magnetic stimulation
Item
patients who have received electroconvulsive therapy or transcranial magnetic stimulation within 6 months prior to screening.
boolean
C0013806 (UMLS CUI [1])
C0436548 (UMLS CUI [2])
C0436548 (UMLS CUI [2])
Epilepsy
Item
patients with a history or seizure disorders.
boolean
C0014544 (UMLS CUI [1])