ID

34979

Description

Blood Test for Breast Cancer Associated Auto Antibodies - Improvement of Octava Blood Test; ODM derived from: https://clinicaltrials.gov/show/NCT02066025

Lien

https://clinicaltrials.gov/show/NCT02066025

Mots-clés

  1. 06/02/2019 06/02/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

6 février 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT02066025

Eligibility Breast Cancer NCT02066025

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female subjects 18 years or over.
Description

Gender | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
subjects following a mammography test.
Description

Mammography

Type de données

boolean

Alias
UMLS CUI [1]
C0024671
subject with pathological evaluation after mammography with birads 3-4-5-6.
Description

Mammography BIRADS

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C1511314
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
female subjects less than 18 years of age
Description

Gender | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
previous or concurrent malignancies
Description

Malignant Neoplasms Previous | Cancer Other

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205156
UMLS CUI [2]
C1707251
autoimmune disorders diagnosed subjects
Description

Autoimmune Diseases

Type de données

boolean

Alias
UMLS CUI [1]
C0004364
hematological malignancies
Description

Hematologic Neoplasms

Type de données

boolean

Alias
UMLS CUI [1]
C0376545
subjects under active chemotherapy treatment or chemotherapy in the past 6 months
Description

Chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
steroid treatment in the past 3 months
Description

Steroid therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0149783
subject undergoing immunosuppressive treatments
Description

Therapeutic immunosuppression

Type de données

boolean

Alias
UMLS CUI [1]
C0021079
subject with verified breast cancer other than invasive ductal or invasive lobular as verified by biopsy/cytology
Description

Breast Carcinoma | Exception Invasive Ductal Breast Carcinoma | Exception Invasive Lobular Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C1134719
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0279565

Similar models

Eligibility Breast Cancer NCT02066025

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
female subjects 18 years or over.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Mammography
Item
subjects following a mammography test.
boolean
C0024671 (UMLS CUI [1])
Mammography BIRADS
Item
subject with pathological evaluation after mammography with birads 3-4-5-6.
boolean
C0024671 (UMLS CUI [1,1])
C1511314 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Gender | Age
Item
female subjects less than 18 years of age
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Malignant Neoplasms Previous | Cancer Other
Item
previous or concurrent malignancies
boolean
C0006826 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1707251 (UMLS CUI [2])
Autoimmune Diseases
Item
autoimmune disorders diagnosed subjects
boolean
C0004364 (UMLS CUI [1])
Hematologic Neoplasms
Item
hematological malignancies
boolean
C0376545 (UMLS CUI [1])
Chemotherapy
Item
subjects under active chemotherapy treatment or chemotherapy in the past 6 months
boolean
C0392920 (UMLS CUI [1])
Steroid therapy
Item
steroid treatment in the past 3 months
boolean
C0149783 (UMLS CUI [1])
Therapeutic immunosuppression
Item
subject undergoing immunosuppressive treatments
boolean
C0021079 (UMLS CUI [1])
Breast Carcinoma | Exception Invasive Ductal Breast Carcinoma | Exception Invasive Lobular Breast Carcinoma
Item
subject with verified breast cancer other than invasive ductal or invasive lobular as verified by biopsy/cytology
boolean
C0678222 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1134719 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0279565 (UMLS CUI [3,2])

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