ID

34162

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01983982

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01983982

Eligibility Breast Cancer NCT01983982

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
female gender
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

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

ID.3

Datatype

boolean

eastern cooperative oncology group performance status 0-2.
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.5

Datatype

boolean

peripheral sensory neuropathy grade 2 or higher.
Beschrijving

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

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

ID.8

Datatype

boolean

pregnant or nursing.
Beschrijving

ID.9

Datatype

boolean

no prior chemotherapy for any reason
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT01983982

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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