ID

38202

Description

A Prospective Longitudinal Breast Cancer Study; ODM derived from: https://clinicaltrials.gov/show/NCT02270931

Lien

https://clinicaltrials.gov/show/NCT02270931

Mots-clés

  1. 27/09/2019 27/09/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

27 septembre 2019

DOI

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Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT02270931

Eligibility Breast Cancer NCT02270931

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females, age≥ 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
histologic/pathologic confirmation of breast cancer
Description

Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0678222
any stage of disease: newly diagnosed, stable, disease progression, surveillance
Description

Disease Newly Diagnosed | Stable Disease | Disease Progression | Surveillance

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1518321
UMLS CUI [2]
C0677946
UMLS CUI [3]
C0242656
UMLS CUI [4]
C0220920
any treatment time point: treatment naïve, currently receiving or completed therapy for breast cancer including active monitoring.
Description

Therapy naive | Therapeutic procedure Breast Carcinoma | Monitoring

Type de données

boolean

Alias
UMLS CUI [1]
C0919936
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0678222
UMLS CUI [3]
C1283169
individuals with a history of malignant disease other than breast cancer that was resected greater than 5 years ago and are currently in remission are eligible.
Description

Malignant Neoplasms In complete remission | Exception Breast Carcinoma Resected

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0677874
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0678222
UMLS CUI [2,3]
C1521996
able to understand and willing to provide informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
males and females, age <18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
no histologic/pathologic confirmation of breast cancer
Description

Confirmation of Breast Carcinoma Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C0521091
UMLS CUI [1,2]
C0678222
UMLS CUI [1,3]
C0332268
any concurrent malignancy other than basal or squamous cell skin cancers, in-situ cervical cancer, or breast cancer.
Description

Cancer Other | Exception Basal cell carcinoma | Exception Squamous cell carcinoma of skin | Exception Carcinoma in situ of uterine cervix | Exception Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0553723
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0851140
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C0678222
treatment plan with fewer than three visits expected in 3 years' time
Description

Treatment Plan Visits Quantity Timespan

Type de données

boolean

Alias
UMLS CUI [1,1]
C0599880
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C1265611
UMLS CUI [1,4]
C0872291
unable to provide informed consent
Description

Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582

Similar models

Eligibility Breast Cancer NCT02270931

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
males and females, age≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma
Item
histologic/pathologic confirmation of breast cancer
boolean
C0678222 (UMLS CUI [1])
Disease Newly Diagnosed | Stable Disease | Disease Progression | Surveillance
Item
any stage of disease: newly diagnosed, stable, disease progression, surveillance
boolean
C0012634 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0677946 (UMLS CUI [2])
C0242656 (UMLS CUI [3])
C0220920 (UMLS CUI [4])
Therapy naive | Therapeutic procedure Breast Carcinoma | Monitoring
Item
any treatment time point: treatment naïve, currently receiving or completed therapy for breast cancer including active monitoring.
boolean
C0919936 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1283169 (UMLS CUI [3])
Malignant Neoplasms In complete remission | Exception Breast Carcinoma Resected
Item
individuals with a history of malignant disease other than breast cancer that was resected greater than 5 years ago and are currently in remission are eligible.
boolean
C0006826 (UMLS CUI [1,1])
C0677874 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1521996 (UMLS CUI [2,3])
Informed Consent
Item
able to understand and willing to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
males and females, age <18 years
boolean
C0001779 (UMLS CUI [1])
Confirmation of Breast Carcinoma Lacking
Item
no histologic/pathologic confirmation of breast cancer
boolean
C0521091 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Cancer Other | Exception Basal cell carcinoma | Exception Squamous cell carcinoma of skin | Exception Carcinoma in situ of uterine cervix | Exception Breast Carcinoma
Item
any concurrent malignancy other than basal or squamous cell skin cancers, in-situ cervical cancer, or breast cancer.
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0553723 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0851140 (UMLS CUI [4,2])
C1705847 (UMLS CUI [5,1])
C0678222 (UMLS CUI [5,2])
Treatment Plan Visits Quantity Timespan
Item
treatment plan with fewer than three visits expected in 3 years' time
boolean
C0599880 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0872291 (UMLS CUI [1,4])
Informed Consent Unable
Item
unable to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])

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