Informações:
Falhas:
ID
21768
Descrição
An Open Trial of Duloxetine on Comorbid Major Depression and Chronic Headache; ODM derived from: https://clinicaltrials.gov/show/NCT00531895
Link
https://clinicaltrials.gov/show/NCT00531895
Palavras-chave
Versões (1)
- 29/04/2017 29/04/2017 -
Transferido a
29 de abril de 2017
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Major Depression NCT00531895
Eligibility Major Depression NCT00531895
- StudyEvent: Eligibility
Similar models
Eligibility Major Depression NCT00531895
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Major Depressive Disorder
Item
major depression (according to dsm-iv criteria)
boolean
C1269683 (UMLS CUI [1])
Montgomery-Asberg Depression Rating Scale Questionnaire
Item
madrs scores superior to 21
boolean
C4054475 (UMLS CUI [1])
Primary Headache Disorder chronic
Item
subjects meeting the international headache society criteria for chronic primary headache (ihsc-2 codes 1.5.1, 1.6.1, 2.3.1, 2.3.2 and 2.4.3) (ichs, 2003)
boolean
C1565106 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,2])
Montgomery-Asberg Depression Rating Scale Questionnaire Reduction Percentage Washout Period
Item
over 50% reduction on madrs scores during wash-out period
boolean
C4054475 (UMLS CUI [1,1])
C0392756 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C1710661 (UMLS CUI [1,4])
C0392756 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C1710661 (UMLS CUI [1,4])
Illicit Drugs Dependence | Alcoholic Intoxication, Chronic
Item
illicit drug or alcohol dependence
boolean
C0086190 (UMLS CUI [1,1])
C0439857 (UMLS CUI [1,2])
C0001973 (UMLS CUI [2])
C0439857 (UMLS CUI [1,2])
C0001973 (UMLS CUI [2])
Multiple allergies | Hypersensitivity duloxetine
Item
history of multiple allergies or hypersensitivity to duloxetine
boolean
C0740281 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0245561 (UMLS CUI [2,2])
C0020517 (UMLS CUI [2,1])
C0245561 (UMLS CUI [2,2])
Epilepsy | nervous system disorder
Item
history of epilepsy or significant neurological disorder
boolean
C0014544 (UMLS CUI [1])
C0027765 (UMLS CUI [2])
C0027765 (UMLS CUI [2])
At risk for suicide
Item
significant suicide risk
boolean
C0563664 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Gender Sexually active | Contraceptive methods Lacking
Item
sexually active female subjects not using an efficient contraceptive method
boolean
C0079399 (UMLS CUI [1,1])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
LABORATORY ABNORMALITIES
Item
significant laboratory abnormalities at baseline
boolean
C1853129 (UMLS CUI [1])
Disease Clinical Significance
Item
significant clinical disease
boolean
C0012634 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
Somatization Disorder | Delusional pain Symptoms
Item
subjects meeting dsm-iv criteria for somatisation disorder. (300.81) or presenting with delusional pain symptoms.
boolean
C0520482 (UMLS CUI [1])
C0394998 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])
C0394998 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])