ID

43638

Beschreibung

Fatigue Caused by Chemotherapy in Women Who Have Undergone Surgery for Breast Cancer and in Healthy Volunteers; ODM derived from: https://clinicaltrials.gov/show/NCT00909662

Link

https://clinicaltrials.gov/show/NCT00909662

Stichworte

Versionen (2)
  1. 26.10.17 26.10.17 -
  2. 20.09.21 20.09.21 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

20. September 2021

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00909662

Englisch

Eligibility Breast Cancer NCT00909662

1 Formulare  
Criteria
Beschreibung

Criteria

meets either of the following criteria:
Beschreibung

Criteria Fulfill

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
has completed surgery for stage i-iii breast cancer and meets the following criteria:
Beschreibung

Operative Surgical Procedures Completed | Breast Carcinoma TNM Breast tumor staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0474926
no bilateral axillary dissection
Beschreibung

Exclusion | Excision of axillary lymph nodes Bilateral

Datentyp

boolean

Alias
UMLS CUI [1]
C2828389
UMLS CUI [2,1]
C0193867
UMLS CUI [2,2]
C0238767
clinically free of active disease
Beschreibung

Disease Free of

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332296
planning to receive adjuvant chemotherapy for operable breast cancer
Beschreibung

Adjuvant Chemotherapy Planned | Breast Carcinoma Operable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0205188
friend or relative of patient matched for age (± 10 years) (control)
Beschreibung

Friend Age matched | Relative Age matched

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0079382
UMLS CUI [1,2]
C0001779
UMLS CUI [1,3]
C0150103
UMLS CUI [2,1]
C0080103
UMLS CUI [2,2]
C0001779
UMLS CUI [2,3]
C0150103
hormone receptor status not specified
Beschreibung

Hormone Receptor Status Unspecified

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Beschreibung

Client Characteristics

Datentyp

boolean

Alias
UMLS CUI [1]
C0815172
known menopausal status
Beschreibung

Menopausal Status Known

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205309
able to read english
Beschreibung

Able to read English Language

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376245
no history of significant cardiovascular disease or stroke, polyneuropathy, amyotrophy, myosthenic syndrome, or pulmonary compromise
Beschreibung

Exclusion Criteria | Cardiovascular Diseases | Cerebrovascular accident | Polyneuropathy | Muscular Atrophy | Myasthenic Syndrome | Pulmonary function impairment

Datentyp

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C0007222
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0152025
UMLS CUI [5]
C0026846
UMLS CUI [6]
C0549225
UMLS CUI [7]
C0858943
prior depression allowed provided that it was not significant
Beschreibung

Depressive disorder

Datentyp

boolean

Alias
UMLS CUI [1]
C0011581
willing to come to the cleveland clinic for 3 assessments
Beschreibung

Assessment Quantity Willing

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1516048
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0600109
prior concurrent therapy:
Beschreibung

Therapeutic procedure

Datentyp

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Beschreibung

ID.15

Datentyp

boolean

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Ähnliche Modelle

Eligibility Breast Cancer NCT00909662

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Criteria Fulfill
Item
meets either of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Operative Surgical Procedures Completed | Breast Carcinoma TNM Breast tumor staging
Item
has completed surgery for stage i-iii breast cancer and meets the following criteria:
boolean
C0543467 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0474926 (UMLS CUI [2,2])
Exclusion | Excision of axillary lymph nodes Bilateral
Item
no bilateral axillary dissection
boolean
C2828389 (UMLS CUI [1])
C0193867 (UMLS CUI [2,1])
C0238767 (UMLS CUI [2,2])
Disease Free of
Item
clinically free of active disease
boolean
C0012634 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
Adjuvant Chemotherapy Planned | Breast Carcinoma Operable
Item
planning to receive adjuvant chemotherapy for operable breast cancer
boolean
C0085533 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0205188 (UMLS CUI [2,2])
Friend Age matched | Relative Age matched
Item
friend or relative of patient matched for age (± 10 years) (control)
boolean
C0079382 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
C0150103 (UMLS CUI [1,3])
C0080103 (UMLS CUI [2,1])
C0001779 (UMLS CUI [2,2])
C0150103 (UMLS CUI [2,3])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Known
Item
known menopausal status
boolean
C3829127 (UMLS CUI [1,1])
C0205309 (UMLS CUI [1,2])
Able to read English Language
Item
able to read english
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Exclusion Criteria | Cardiovascular Diseases | Cerebrovascular accident | Polyneuropathy | Muscular Atrophy | Myasthenic Syndrome | Pulmonary function impairment
Item
no history of significant cardiovascular disease or stroke, polyneuropathy, amyotrophy, myosthenic syndrome, or pulmonary compromise
boolean
C0680251 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0152025 (UMLS CUI [4])
C0026846 (UMLS CUI [5])
C0549225 (UMLS CUI [6])
C0858943 (UMLS CUI [7])
Depressive disorder
Item
prior depression allowed provided that it was not significant
boolean
C0011581 (UMLS CUI [1])
Assessment Quantity Willing
Item
willing to come to the cleveland clinic for 3 assessments
boolean
C1516048 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.15
Item
see disease characteristics
boolean
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