ID

34162

Description

Effect of Chemotherapy on Pain Sensitivity and Patient-reported Symptoms; ODM derived from: https://clinicaltrials.gov/show/NCT01983982

Link

https://clinicaltrials.gov/show/NCT01983982

Keywords

  1. 1/14/19 1/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 14, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01983982

Eligibility Breast Cancer NCT01983982

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female gender
Description

ID.1

Data type

boolean

histologically proven stage i-iii invasive carcinoma of the breast who is planning to receive a standard dose of adjuvant chemotherapy.
Description

ID.2

Data type

boolean

surgical resection should be complete at the time of study enrollment.
Description

ID.3

Data type

boolean

eastern cooperative oncology group performance status 0-2.
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
average pain over the past 24 hours of 4 or greater on a 0-10 scale.
Description

ID.5

Data type

boolean

peripheral sensory neuropathy grade 2 or higher.
Description

ID.6

Data type

boolean

personal history of schizophrenia or major depressive disorder, or history of suicidal ideation or attempt within the past 2 years.
Description

ID.7

Data type

boolean

thumbnail abnormalities on either hand (such as artificial nails) that are likely to alter pain perception during testing.
Description

ID.8

Data type

boolean

pregnant or nursing.
Description

ID.9

Data type

boolean

no prior chemotherapy for any reason
Description

ID.10

Data type

boolean

Similar models

Eligibility Breast Cancer NCT01983982

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
female gender
boolean
ID.2
Item
histologically proven stage i-iii invasive carcinoma of the breast who is planning to receive a standard dose of adjuvant chemotherapy.
boolean
ID.3
Item
surgical resection should be complete at the time of study enrollment.
boolean
ID.4
Item
eastern cooperative oncology group performance status 0-2.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
average pain over the past 24 hours of 4 or greater on a 0-10 scale.
boolean
ID.6
Item
peripheral sensory neuropathy grade 2 or higher.
boolean
ID.7
Item
personal history of schizophrenia or major depressive disorder, or history of suicidal ideation or attempt within the past 2 years.
boolean
ID.8
Item
thumbnail abnormalities on either hand (such as artificial nails) that are likely to alter pain perception during testing.
boolean
ID.9
Item
pregnant or nursing.
boolean
ID.10
Item
no prior chemotherapy for any reason
boolean

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