Informações:
Falhas:
ID
20536
Descrição
Evaluating the Effectiveness of Escitalopram to Prevent Depression in Head and Neck Cancer Patients Receiving Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT00536172
Link
https://clinicaltrials.gov/show/NCT00536172
Palavras-chave
Versões (1)
- 02/03/2017 02/03/2017 -
Transferido a
2 de março de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Depression NCT00536172
Eligibility Depression NCT00536172
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT00536172
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
newly diagnosed or recurrent epidermoid cancer of the head and neck
Item
newly diagnosed or recurrent epidermoid cancer of the head and neck
boolean
C1168401 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0277556 (UMLS CUI [1,3])
C1518321 (UMLS CUI [1,2])
C0277556 (UMLS CUI [1,3])
requires more than minimal therapy for treatment
Item
requires more than minimal therapy for treatment
boolean
C0332121 (UMLS CUI [1,1])
C1168401 (UMLS CUI [1,2])
C1168401 (UMLS CUI [1,2])
english
Item
able to read and write in english
boolean
C0376245 (UMLS CUI [1])
contraceptive methods
Item
willing to use an effective form of birth control throughout the study
boolean
C0700589 (UMLS CUI [1])
Major Depressive Disorder | Schizophrenia | Bipolar Disorder
Item
meets mini criteria for major depression, schizophrenia, or bipolar illness or scores 24 or less
boolean
C1269683 (UMLS CUI [1])
C0036341 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
C0036341 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
suicidal or psychotic
Item
suicidal or psychotic
boolean
C0438696 (UMLS CUI [1])
C0871189 (UMLS CUI [2])
C0871189 (UMLS CUI [2])
Hypersensitivity; Citalopram | Hypersensitivity; Selective Serotonin Reuptake Inhibitors
Item
current allergy or hypersensitivity to citalopram or other ssris
boolean
C0020517 (UMLS CUI [1,1])
C0008845 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0360105 (UMLS CUI [2,2])
C0008845 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0360105 (UMLS CUI [2,2])
treated with monoamine oxidase inhibitors
Item
treated with monoamine oxidase inhibitors 14 days prior to study entry
boolean
C0026457 (UMLS CUI [1])
antidepressive agents
Item
use of antidepressants within 1 week of study entry
boolean
C0003289 (UMLS CUI [1])
pregnancy, breastfeeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Medical History; neoplasm/cancer surgery | Prior Chemotherapy | prior radiation therapy
Item
history of an adequate cancer operation, radiation, or chemotherapy within 6 months of study entry
boolean
C0262926 (UMLS CUI [1,1])
C0597029 (UMLS CUI [1,2])
C1514457 (UMLS CUI [2])
C0279134 (UMLS CUI [3])
C0597029 (UMLS CUI [1,2])
C1514457 (UMLS CUI [2])
C0279134 (UMLS CUI [3])
melanoma or lymphoma cancer of the head and neck
Item
diagnosed with melanoma or lymphoma cancer of the head and neck
boolean
C0587060 (UMLS CUI [1])
C0432556 (UMLS CUI [2])
C0432556 (UMLS CUI [2])
study subject participation status
Item
currently participating in another research study involving a therapeutic intervention
boolean
C2348568 (UMLS CUI [1])