ID

20536

Description

Evaluating the Effectiveness of Escitalopram to Prevent Depression in Head and Neck Cancer Patients Receiving Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT00536172

Lien

https://clinicaltrials.gov/show/NCT00536172

Mots-clés

  1. 02/03/2017 02/03/2017 -
Téléchargé le

2 mars 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Depression NCT00536172

Eligibility Depression NCT00536172

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT00536172
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
newly diagnosed or recurrent epidermoid cancer of the head and neck
Description

newly diagnosed or recurrent epidermoid cancer of the head and neck

Type de données

boolean

Alias
UMLS CUI [1,1]
C1168401
UMLS CUI [1,2]
C1518321
UMLS CUI [1,3]
C0277556
requires more than minimal therapy for treatment
Description

requires more than minimal therapy for treatment

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332121
UMLS CUI [1,2]
C1168401
able to read and write in english
Description

english

Type de données

boolean

Alias
UMLS CUI [1]
C0376245
willing to use an effective form of birth control throughout the study
Description

contraceptive methods

Type de données

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
meets mini criteria for major depression, schizophrenia, or bipolar illness or scores 24 or less
Description

Major Depressive Disorder | Schizophrenia | Bipolar Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C1269683
UMLS CUI [2]
C0036341
UMLS CUI [3]
C0005586
suicidal or psychotic
Description

suicidal or psychotic

Type de données

boolean

Alias
UMLS CUI [1]
C0438696
UMLS CUI [2]
C0871189
current allergy or hypersensitivity to citalopram or other ssris
Description

Hypersensitivity; Citalopram | Hypersensitivity; Selective Serotonin Reuptake Inhibitors

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0008845
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0360105
treated with monoamine oxidase inhibitors 14 days prior to study entry
Description

treated with monoamine oxidase inhibitors

Type de données

boolean

Alias
UMLS CUI [1]
C0026457
use of antidepressants within 1 week of study entry
Description

antidepressive agents

Type de données

boolean

Alias
UMLS CUI [1]
C0003289
pregnant or breastfeeding
Description

pregnancy, breastfeeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
history of an adequate cancer operation, radiation, or chemotherapy within 6 months of study entry
Description

Medical History; neoplasm/cancer surgery | Prior Chemotherapy | prior radiation therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0597029
UMLS CUI [2]
C1514457
UMLS CUI [3]
C0279134
diagnosed with melanoma or lymphoma cancer of the head and neck
Description

melanoma or lymphoma cancer of the head and neck

Type de données

boolean

Alias
UMLS CUI [1]
C0587060
UMLS CUI [2]
C0432556
currently participating in another research study involving a therapeutic intervention
Description

study subject participation status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Depression NCT00536172

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT00536172
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
suicidal or psychotic
Item
suicidal or psychotic
boolean
C0438696 (UMLS CUI [1])
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])
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])
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])
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])
study subject participation status
Item
currently participating in another research study involving a therapeutic intervention
boolean
C2348568 (UMLS CUI [1])

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