Information:
Fel:
ID
38246
Beskrivning
Exclusive Intraoperative Radiation Therapy for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01276938
Länk
https://clinicaltrials.gov/show/NCT01276938
Nyckelord
Versioner (1)
- 2019-10-02 2019-10-02 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
2 oktober 2019
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT01276938
Eligibility Breast Neoplasms NCT01276938
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasms NCT01276938
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Breast Carcinoma epithelial | Exception Lobular Carcinoma | Quadrantectomy of breast
Item
non lobular epithelial breast carcinoma, excised with standard quadrantectomy
boolean
C0678222 (UMLS CUI [1,1])
C0221908 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0206692 (UMLS CUI [2,2])
C0337354 (UMLS CUI [3])
C0221908 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0206692 (UMLS CUI [2,2])
C0337354 (UMLS CUI [3])
Age
Item
age ≥ 45 and < 85
boolean
C0001779 (UMLS CUI [1])
Neoplasm Major Diameter
Item
tumor major diameter ≤ 2.5 cm
boolean
C0027651 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0205164 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
Negative Surgical Margin
Item
negative surgical margins (≥ 5 mm)
boolean
C1709157 (UMLS CUI [1])
Follow-up Willing
Item
willingness to undergo follow up examinations
boolean
C3274571 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,2])
Imaging Willing | MRI | Mammography | Ultrasonography
Item
willingness to undergo imaging examinations (mri, mammograms, ultrasonography)
boolean
C0011923 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2])
C0024671 (UMLS CUI [3])
C0041618 (UMLS CUI [4])
C0600109 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2])
C0024671 (UMLS CUI [3])
C0041618 (UMLS CUI [4])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Ductal carcinoma in situ | Carcinoma, Lobular
Item
ductal carcinoma in situ or lobular carcinoma
boolean
C0007124 (UMLS CUI [1])
C0206692 (UMLS CUI [2])
C0206692 (UMLS CUI [2])
Extensive Intraductal Component Percentage | Ductal Carcinoma In Situ with Microinvasion
Item
extensive intraductal component (greater than 25%) or intraductal carcinoma with microinvasion
boolean
C1882485 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C2732473 (UMLS CUI [2])
C0439165 (UMLS CUI [1,2])
C2732473 (UMLS CUI [2])
Comorbidity Serious | Condition Excludes Protocol Compliance | Disease Excludes Protocol Compliance | Mental disorders | Addictive Behavior
Item
serious concomitant disease or any disorder or condition (such as psychiatric or addictive disorders) that, in the opinion of the investigator, would preclude the patient from meeting the study requirements
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0348080 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0525058 (UMLS CUI [3,3])
C0004936 (UMLS CUI [4])
C0085281 (UMLS CUI [5])
C0205404 (UMLS CUI [1,2])
C0348080 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0525058 (UMLS CUI [3,3])
C0004936 (UMLS CUI [4])
C0085281 (UMLS CUI [5])
Pregnancy | Breast Feeding | Contraceptive Device as needed
Item
pregnancy or lactation at the time of enrolment proposal (if necessary, during the trial patients must use effective contraceptive device)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0009886 (UMLS CUI [3,1])
C1555334 (UMLS CUI [3,2])
C0006147 (UMLS CUI [2])
C0009886 (UMLS CUI [3,1])
C1555334 (UMLS CUI [3,2])
Collagen-vascular disease
Item
collagen vascular disorders
boolean
C0262428 (UMLS CUI [1])