ID

44228

Description

Comparison of Whole Breast Screening Ultrasound and Contrast Enhanced Mammography for Supplemental Breast Cancer Screening; ODM derived from: https://clinicaltrials.gov/show/NCT02310698

Lien

https://clinicaltrials.gov/show/NCT02310698

Mots-clés

Versions (2)
  1. 13/02/2019 13/02/2019 -
  2. 20/09/2021 20/09/2021 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Breast Cancer Screening NCT02310698

Anglais

Eligibility Breast Cancer Screening NCT02310698

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women scheduled for screening wbus and a screening ffdm on the same day or within the following 30 days of each other
Description

Gender | Whole Ultrasound screening of breast Scheduled | Full field digital mammogram Scheduled

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C2367051
UMLS CUI [2,2]
C0439751
UMLS CUI [2,3]
C0205539
UMLS CUI [3,1]
C3862913
UMLS CUI [3,2]
C0205539
women scheduled for screening cedm alone
Description

Gender | Contrast enhanced digital mammography Scheduled

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C4511913
UMLS CUI [2,2]
C0205539
women scheduled for wbus and screening cedm on the same day or within 30 days of one another
Description

Gender | Whole Ultrasound screening of breast Scheduled | Contrast enhanced digital mammography Scheduled

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C2367051
UMLS CUI [2,2]
C0439751
UMLS CUI [2,3]
C0205539
UMLS CUI [3,1]
C4511913
UMLS CUI [3,2]
C0205539
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 30 years old
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
male patients
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
patients with any clinical breast symptoms (palpable mass, nipple discharge, etc)
Description

Breast symptoms | Palpable mass | Nipple discharge

Type de données

boolean

Alias
UMLS CUI [1]
C2220038
UMLS CUI [2]
C0746412
UMLS CUI [3]
C0149741
patients with known diagnosis of breast cancer
Description

Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0678222
patients with any breast surgery or biopsy within 90 days prior to the study
Description

Operation on breast | Biopsy of breast

Type de données

boolean

Alias
UMLS CUI [1]
C3714726
UMLS CUI [2]
C0405352
patients who have had a lumpectomy for breast cancer within 3 years prior to the study
Description

Segmental Mastectomy Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024885
UMLS CUI [1,2]
C0678222
patients who are thought to have a breast mri within 3 years prior to the study
Description

Magnetic resonance imaging of breast

Type de données

boolean

Alias
UMLS CUI [1]
C0344104
patients with breast implants on the breast that is being imaged
Description

Breast implants | Breast Imaging

Type de données

boolean

Alias
UMLS CUI [1]
C0179412
UMLS CUI [2,1]
C0006141
UMLS CUI [2,2]
C0011923
patients with contraindication to the intravenous use of iodinated contrast agent (i.e. allergy to iodinated contrast or severely impaired renal function with a creatinine level ≥1.3)
Description

Medical contraindication Iodinated contrast agent Intravenous use | Hypersensitivity Iodinated contrast media | Renal Insufficiency Severe | Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0879373
UMLS CUI [1,3]
C1522726
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1960405
UMLS CUI [3,1]
C1565489
UMLS CUI [3,2]
C0205082
UMLS CUI [4]
C0201976
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Similar models

Eligibility Breast Cancer Screening NCT02310698

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Whole Ultrasound screening of breast Scheduled | Full field digital mammogram Scheduled
Item
women scheduled for screening wbus and a screening ffdm on the same day or within the following 30 days of each other
boolean
C0079399 (UMLS CUI [1])
C2367051 (UMLS CUI [2,1])
C0439751 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C3862913 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Gender | Contrast enhanced digital mammography Scheduled
Item
women scheduled for screening cedm alone
boolean
C0079399 (UMLS CUI [1])
C4511913 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Gender | Whole Ultrasound screening of breast Scheduled | Contrast enhanced digital mammography Scheduled
Item
women scheduled for wbus and screening cedm on the same day or within 30 days of one another
boolean
C0079399 (UMLS CUI [1])
C2367051 (UMLS CUI [2,1])
C0439751 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C4511913 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
age < 30 years old
boolean
C0001779 (UMLS CUI [1])
Gender
Item
male patients
boolean
C0079399 (UMLS CUI [1])
Breast symptoms | Palpable mass | Nipple discharge
Item
patients with any clinical breast symptoms (palpable mass, nipple discharge, etc)
boolean
C2220038 (UMLS CUI [1])
C0746412 (UMLS CUI [2])
C0149741 (UMLS CUI [3])
Breast Carcinoma
Item
patients with known diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Operation on breast | Biopsy of breast
Item
patients with any breast surgery or biopsy within 90 days prior to the study
boolean
C3714726 (UMLS CUI [1])
C0405352 (UMLS CUI [2])
Segmental Mastectomy Breast Carcinoma
Item
patients who have had a lumpectomy for breast cancer within 3 years prior to the study
boolean
C0024885 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Magnetic resonance imaging of breast
Item
patients who are thought to have a breast mri within 3 years prior to the study
boolean
C0344104 (UMLS CUI [1])
Breast implants | Breast Imaging
Item
patients with breast implants on the breast that is being imaged
boolean
C0179412 (UMLS CUI [1])
C0006141 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
Medical contraindication Iodinated contrast agent Intravenous use | Hypersensitivity Iodinated contrast media | Renal Insufficiency Severe | Creatinine measurement, serum
Item
patients with contraindication to the intravenous use of iodinated contrast agent (i.e. allergy to iodinated contrast or severely impaired renal function with a creatinine level ≥1.3)
boolean
C1301624 (UMLS CUI [1,1])
C0879373 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C1960405 (UMLS CUI [2,2])
C1565489 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0201976 (UMLS CUI [4])
Retour au début de la page 

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