Informazione:
Errore:
ID
14861
Descrizione
SAVI SCOUT Clinical Evaluation Study; ODM derived from: https://clinicaltrials.gov/show/NCT02370082
collegamento
https://clinicaltrials.gov/show/NCT02370082
Keywords
versioni (1)
- 02/05/16 02/05/16 -
Caricato su
2 maggio 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Breast Neoplasm NCT02370082
Eligibility Breast Neoplasm NCT02370082
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasm NCT02370082
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Lesion of breast Palpable | Requirement Excision
Item
• patient has a non-palpable breast lesion that requires excision
boolean
C0567489 (UMLS CUI [1,1])
C0522499 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C0728940 (UMLS CUI [2,2])
C0522499 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C0728940 (UMLS CUI [2,2])
Depth of lesion Surface of skin | Supine Position
Item
lesion depth ≤ 3 cm from the skin surface in the supine position
boolean
C1827571 (UMLS CUI [1,1])
C1180212 (UMLS CUI [1,2])
C0038846 (UMLS CUI [2])
C1180212 (UMLS CUI [1,2])
C0038846 (UMLS CUI [2])
Scheduled Excision | Scheduled Breast-Conserving Surgery
Item
patient is scheduled for excision or bct at a participating institution
boolean
C0205539 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C0205539 (UMLS CUI [2,1])
C0917927 (UMLS CUI [2,2])
C0728940 (UMLS CUI [1,2])
C0205539 (UMLS CUI [2,1])
C0917927 (UMLS CUI [2,2])
Age
Item
patient is between the ages of 18 and 90 years
boolean
C0001779 (UMLS CUI [1])
Gender
Item
patient is female
boolean
C0079399 (UMLS CUI [1])
Compliance behavior | Availability of follow-up
Item
patient is willing and able to comply with all study procedures and be available to follow-up for the duration of the study
boolean
C1321605 (UMLS CUI [1])
C0470187 (UMLS CUI [2,1])
C1522577 (UMLS CUI [2,2])
C0470187 (UMLS CUI [2,1])
C1522577 (UMLS CUI [2,2])
Localization of lesion of breast | Coronal
Item
for lesions requiring multiple reflectors for localization, they must allow for reflectors to be placed ≥ 1cm from one another relative to the coronal plane subject exclusion criteria
boolean
C0842739 (UMLS CUI [1])
C0205123 (UMLS CUI [2])
C0205123 (UMLS CUI [2])
Study Subject Participation Status
Item
an individual who meets any of the following criteria will be excluded from participation in this study:
boolean
C2348568 (UMLS CUI [1])
Breast Carcinoma Ipsilateral Previous
Item
patient had a previous ipsilateral breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0441989 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0441989 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
Multicentric Breast Carcinoma
Item
patient has multicentric breast cancer
boolean
C2986664 (UMLS CUI [1])
Carcinoma breast stage IV
Item
patient has stage iv breast cancer
boolean
C0278488 (UMLS CUI [1])
Neoadjuvant Therapy Chemotherapy
Item
patient has been treated with neoadjuvant chemotherapy
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
patient is pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])