Informations:
Erreur:
ID
33638
Description
The Establishment of the Objective Diagnostic Markers and Personalized Medical Intervention in Patients With Major Depressive Disorders (MDD); ODM derived from: https://clinicaltrials.gov/show/NCT02023567
Lien
https://clinicaltrials.gov/show/NCT02023567
Mots-clés
Versions (1)
- 17/12/2018 17/12/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
17 décembre 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Depressive Disorder, Major NCT02023567
Eligibility Depressive Disorder, Major NCT02023567
- StudyEvent: Eligibility
Similar models
Eligibility Depressive Disorder, Major NCT02023567
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age
Item
age between 18-55, male or female;
boolean
C0001779 (UMLS CUI [1])
Major Depressive Disorder
Item
the diagnosis of mdd consistent with dsm-iv (m.i.n.i)
boolean
C1269683 (UMLS CUI [1])
First episode | Recurrent disease
Item
first-episode or relapsed;
boolean
C0439615 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
C0277556 (UMLS CUI [2])
Able to read | Able to write | Questionnaire Completion | Psychological assessment Completion
Item
certain ability of reading and writing to complete the questionnaire survey and psychological assessment.
boolean
C0586740 (UMLS CUI [1])
C0584993 (UMLS CUI [2])
C0034394 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C0204452 (UMLS CUI [4,1])
C0205197 (UMLS CUI [4,2])
C0584993 (UMLS CUI [2])
C0034394 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C0204452 (UMLS CUI [4,1])
C0205197 (UMLS CUI [4,2])
Informed Consent
Item
all participants provide written confirmation of informed consent prior to engaging the study protocol.
boolean
C0021430 (UMLS CUI [1])
Condition Neurologic | Substance Dependence | Impaired cognition
Item
current psychopathology or a history of neurologic conditions, including alcohol/substances dependence, the diagnosis of cognition impairment;
boolean
C0348080 (UMLS CUI [1,1])
C0205494 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2])
C0338656 (UMLS CUI [3])
C0205494 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2])
C0338656 (UMLS CUI [3])
Disease Somatic Severe | Cardiovascular Diseases Severe | Cerebrovascular Disorders Severe | Respiration Disorders Severe | Liver diseases Severe | Kidney Diseases Severe | Malignant Neoplasms
Item
severe somatic diseases, such as severe cardio-cerebral vascular diseases, respiratory diseases, liver diseases, kidney diseases, or malignant tumors;
boolean
C0012634 (UMLS CUI [1,1])
C2986476 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0007222 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0007820 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0035204 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0023895 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0022658 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
C0006826 (UMLS CUI [7])
C2986476 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0007222 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0007820 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0035204 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0023895 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0022658 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
C0006826 (UMLS CUI [7])
Informed Consent Lacking
Item
not signed the informed consent;
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Study Subject Participation Status
Item
been engaging other studies.
boolean
C2348568 (UMLS CUI [1])