ID

34162

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01983982

Nyckelord

  1. 2019-01-14 2019-01-14 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

14 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01983982

Eligibility Breast Cancer NCT01983982

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
female gender
Beskrivning

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

eastern cooperative oncology group performance status 0-2.
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.5

Datatyp

boolean

peripheral sensory neuropathy grade 2 or higher.
Beskrivning

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

pregnant or nursing.
Beskrivning

ID.9

Datatyp

boolean

no prior chemotherapy for any reason
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT01983982

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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