ID

44228

Descrição

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

Link

https://clinicaltrials.gov/show/NCT02310698

Palavras-chave

Versões (2)
  1. 13/02/2019 13/02/2019 -
  2. 20/09/2021 20/09/2021 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

20 de setembro de 2021

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Breast Cancer Screening NCT02310698

Inglês

Eligibility Breast Cancer Screening NCT02310698

1 Formulários  
Inclusion Criteria
Descrição

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
Descrição

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

Tipo de dados

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
Descrição

Gender | Contrast enhanced digital mammography Scheduled

Tipo de dados

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
Descrição

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

Tipo de dados

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
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 30 years old
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
male patients
Descrição

Gender

Tipo de dados

boolean

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

Breast symptoms | Palpable mass | Nipple discharge

Tipo de dados

boolean

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

Breast Carcinoma

Tipo de dados

boolean

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

Operation on breast | Biopsy of breast

Tipo de dados

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
Descrição

Segmental Mastectomy Breast Carcinoma

Tipo de dados

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
Descrição

Magnetic resonance imaging of breast

Tipo de dados

boolean

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

Breast implants | Breast Imaging

Tipo de dados

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)
Descrição

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

Tipo de dados

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
Voltar ao início da página

Similar models

Eligibility Breast Cancer Screening NCT02310698

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial