Información:
Error:
ID
33895
Descripción
The Measurement-based Care in Patients With Depressive Disorder: A Randomized Controlled Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02191124
Link
https://clinicaltrials.gov/show/NCT02191124
Palabras clave
Versiones (1)
- 6/1/19 6/1/19 -
Titular de derechos de autor
See clinicaltrials.gov
Subido en
6 de enero de 2019
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT02191124
Eligibility Major Depressive Disorder NCT02191124
- StudyEvent: Eligibility
Similar models
Eligibility Major Depressive Disorder NCT02191124
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Age
Item
1. age 18-65 years;
boolean
C0001779 (UMLS CUI [1])
Outpatients
Item
2. outpatients;
boolean
C0029921 (UMLS CUI [1])
DEPRESSIVE DISORDER MAJOR WITHOUT PSYCHOTIC FEATURE
Item
3. diagnosis of non-psychotic mdd established by treating psychiatrists and confirmed by a checklist based on dsm-iv criteria at study entry ;
boolean
C0743081 (UMLS CUI [1])
Hamilton Depression Rating Scale 17 Item Clinical Classification
Item
4. total score of hamd-17≥17;
boolean
C3639712 (UMLS CUI [1])
Able to communicate | Informed Consent
Item
5. ability to communicate and provide written consent.
boolean
C2364293 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
Substance Dependence | Bipolar Disorder | Psychotic Disorders | Obsessive-Compulsive Disorder | Eating Disorders
Item
1. current or past history of drug and alcohol dependence, bipolar, psychotic, obsessive-compulsive, or eating disorders;
boolean
C0038580 (UMLS CUI [1])
C0005586 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
C0028768 (UMLS CUI [4])
C0013473 (UMLS CUI [5])
C0005586 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
C0028768 (UMLS CUI [4])
C0013473 (UMLS CUI [5])
Unresponsive to Antidepressive Agents Quantity | Intolerance to Antidepressive Agents Quantity | Unresponsive to Paroxetine | Intolerance to Paroxetine | Unresponsive to Mirtazapine | Intolerance to Mirtazapine
Item
2. history of lack of response or intolerance to any of the two protocol antidepressants (paroxetine or mirtazapine);
boolean
C0205269 (UMLS CUI [1,1])
C0003289 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1744706 (UMLS CUI [2,1])
C0003289 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0205269 (UMLS CUI [3,1])
C0070122 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C0070122 (UMLS CUI [4,2])
C0205269 (UMLS CUI [5,1])
C0049506 (UMLS CUI [5,2])
C1744706 (UMLS CUI [6,1])
C0049506 (UMLS CUI [6,2])
C0003289 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1744706 (UMLS CUI [2,1])
C0003289 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0205269 (UMLS CUI [3,1])
C0070122 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C0070122 (UMLS CUI [4,2])
C0205269 (UMLS CUI [5,1])
C0049506 (UMLS CUI [5,2])
C1744706 (UMLS CUI [6,1])
C0049506 (UMLS CUI [6,2])
Pregnancy | Breast Feeding
Item
3. being pregnant or breast-feeding;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Suicide attempt | Depressive episode | Medical condition Major | Antidepressive Agents Contraindicated
Item
4. suicide attempts in the current depressive episode or major medical conditions contraindicating the use of the protocol antidepressants.
boolean
C0038663 (UMLS CUI [1])
C0349217 (UMLS CUI [2])
C3843040 (UMLS CUI [3,1])
C0205164 (UMLS CUI [3,2])
C0003289 (UMLS CUI [4,1])
C1444657 (UMLS CUI [4,2])
C0349217 (UMLS CUI [2])
C3843040 (UMLS CUI [3,1])
C0205164 (UMLS CUI [3,2])
C0003289 (UMLS CUI [4,1])
C1444657 (UMLS CUI [4,2])