Informazione:
Errore:
ID
16452
Descrizione
A Pilot Study Evaluation of the Efficacy of SonoVue to Detect and Characterise Breast Lesions; ODM derived from: https://clinicaltrials.gov/show/NCT00243698
collegamento
https://clinicaltrials.gov/show/NCT00243698
Keywords
versioni (1)
- 17/07/16 17/07/16 -
Caricato su
17 luglio 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Breast Tumors NCT00243698
Eligibility Breast Tumors NCT00243698
- StudyEvent: Eligibility
Similar models
Eligibility Breast Tumors NCT00243698
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
enlarging fibroadenoma, suspect malignant nodule, microcalcification or a malignant nodule
Item
woman presenting with: enlarging fibroadenoma (less than 2 cm in diameter or woman over 40 years old with fibroadenoma less than 2 cm in diameter) or suspect malignant nodule (less than 2 cm in diameter) or a cluster of microcalcification or a malignant nodule (size greater than 3 cm) diagnosed with mammography and/or mri and/or united states (us) examination performed within 1 month before the study.
boolean
C0178421 (UMLS CUI [1])
C0948627 (UMLS CUI [2])
C0520594 (UMLS CUI [3])
C0948627 (UMLS CUI [2])
C0520594 (UMLS CUI [3])
biopsy or surgery
Item
woman scheduled for biopsy or surgery within 1 month from the examination.
boolean
C0405352 (UMLS CUI [1])
C3714726 (UMLS CUI [2])
C3714726 (UMLS CUI [2])
biopsy on the lesion
Item
patients who have already performed a biopsy on the lesion during investigation
boolean
C0405352 (UMLS CUI [1])
contraindication to perform a contrast-enhanced mri examination
Item
any contraindication to perform a contrast-enhanced mri examination for the patients presenting with a malignant nodule (size greater than 3 cm)
boolean
C0522473 (UMLS CUI [1,1])
C1707501 (UMLS CUI [1,2])
C1707501 (UMLS CUI [1,2])
investigational drug, study subject participation status
Item
patients previously entered in this study or having received an investigational drug within 30 days prior to admission to this study
boolean
C0013230 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
C2348568 (UMLS CUI [2])
comorbidities
Item
patients with any medical condition or other circumstances which would significantly decrease the chances of obtaining reliable data or of achieving the study objectives (drug dependence, psychiatric disorders, dementia or other reasons)
boolean
C0009488 (UMLS CUI [1])
pregnant or nursing female
Item
pregnant or nursing female
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
coronary syndrome
Item
patient known to have a coronary syndrome
boolean
C0948089 (UMLS CUI [1])
unstable angina and myocardial infarction
Item
unstable angina and myocardial infarction
boolean
C0002965 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0027051 (UMLS CUI [2])
acute cardiac failure
Item
acute cardiac failure, class iii/iv cardiac failure
boolean
C0264714 (UMLS CUI [1])
arrhythmia
Item
severe rhythm disorders
boolean
C0003811 (UMLS CUI [1])
acute endocarditis
Item
acute endocarditis
boolean
C0014118 (UMLS CUI [1])
prosthetic valves
Item
prosthetic valves
boolean
C0336548 (UMLS CUI [1])