ID

29271

Beschreibung

Digital Breast Tomosynthesis Versus Contrast Enhanced Magnetic Resonance Imaging (MRI) for Breast Cancer Staging; ODM derived from: https://clinicaltrials.gov/show/NCT01060085

Link

https://clinicaltrials.gov/show/NCT01060085

Stichworte

  1. 15.03.18 15.03.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

15. März 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Ductal Carcinoma In Situ NCT01060085

Eligibility Ductal Carcinoma In Situ NCT01060085

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is female of any race and ethnicity
Beschreibung

Gender | Racial group Any | Ethnicity Any

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0034510
UMLS CUI [2,2]
C1552551
UMLS CUI [3,1]
C0015031
UMLS CUI [3,2]
C1552551
subject is at least 30 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
subject has histologically proven dcis or invasive breast carcinoma.
Beschreibung

Noninfiltrating Intraductal Carcinoma | Invasive carcinoma of breast

Datentyp

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2]
C0853879
subject is able to undergo cemri at dhmc-lebanon
Beschreibung

Contrast-enhanced Magnetic Resonance Imaging Medical center Specified

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1707501
UMLS CUI [1,2]
C0565990
UMLS CUI [1,3]
C0205369
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are pregnant or think they may be pregnant
Beschreibung

Pregnancy | Possible pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0425965
patients who are breast-feeding.
Beschreibung

Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0006147
patients who have significant existing breast trauma
Beschreibung

Breast Trauma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0006141
UMLS CUI [1,2]
C3714660
subjects unable or unwilling to undergo informed consent
Beschreibung

Informed Consent Unable | Informed Consent Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
absolute contraindication to cemri, including:
Beschreibung

Medical contraindication Contrast-enhanced Magnetic Resonance Imaging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1707501
1. presence of implanted electrical device (pacemaker or neurostimulator),aneurysm clip, or metallic foreign body in or near the eyes
Beschreibung

Implant Electrical | Artificial cardiac pacemaker | Neurostimulator | Aneurysm clip | Metallic foreign body Intraocular | Metallic foreign body Nearby Eye

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021102
UMLS CUI [1,2]
C0442828
UMLS CUI [2]
C0030163
UMLS CUI [3]
C0582124
UMLS CUI [4]
C0179977
UMLS CUI [5,1]
C1720389
UMLS CUI [5,2]
C3282905
UMLS CUI [6,1]
C1720389
UMLS CUI [6,2]
C1706276
UMLS CUI [6,3]
C0015392
2. life threatening allergy to gadolinium contrast
Beschreibung

Hypersensitivity Life Threatening Gadolinium-based Contrast Agent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C2826244
UMLS CUI [1,3]
C3249258
cemri performed at institution other than dhmc lebanon
Beschreibung

Contrast-enhanced Magnetic Resonance Imaging Performed | Exception Medical center Specified

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1707501
UMLS CUI [1,2]
C0884358
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0565990
UMLS CUI [2,3]
C0205369
patients undergoing neoadjuvant therapy
Beschreibung

Neoadjuvant Therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0600558
patients with maximum tumor diameter >5cm
Beschreibung

Tumor Diameter Size Maximum

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C1301886
UMLS CUI [1,3]
C0456389
UMLS CUI [1,4]
C0806909
patients presenting with inflammatory breast cancer
Beschreibung

Inflammatory Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1]
C0278601
patients with gross axillary lymphadenopathy on clinical exam or by imaging
Beschreibung

Axillary lymphadenopathy Gross Medical Examination | Axillary lymphadenopathy Gross Imaging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0578735
UMLS CUI [1,2]
C0439806
UMLS CUI [1,3]
C0582103
UMLS CUI [2,1]
C0578735
UMLS CUI [2,2]
C0439806
UMLS CUI [2,3]
C0011923
maximum breast size limitation: i.e. breast size that exceeds the size of the large format image receptor (24cm x 29cm) on any view
Beschreibung

Breast Size Maximum Limitation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0425782
UMLS CUI [1,2]
C0806909
UMLS CUI [1,3]
C0449295

Ähnliche Modelle

Eligibility Ductal Carcinoma In Situ NCT01060085

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Racial group Any | Ethnicity Any
Item
subject is female of any race and ethnicity
boolean
C0079399 (UMLS CUI [1])
C0034510 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0015031 (UMLS CUI [3,1])
C1552551 (UMLS CUI [3,2])
Age
Item
subject is at least 30 years old
boolean
C0001779 (UMLS CUI [1])
Noninfiltrating Intraductal Carcinoma | Invasive carcinoma of breast
Item
subject has histologically proven dcis or invasive breast carcinoma.
boolean
C0007124 (UMLS CUI [1])
C0853879 (UMLS CUI [2])
Contrast-enhanced Magnetic Resonance Imaging Medical center Specified
Item
subject is able to undergo cemri at dhmc-lebanon
boolean
C1707501 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Possible pregnancy
Item
patients who are pregnant or think they may be pregnant
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])
Breast Feeding
Item
patients who are breast-feeding.
boolean
C0006147 (UMLS CUI [1])
Breast Trauma
Item
patients who have significant existing breast trauma
boolean
C0006141 (UMLS CUI [1,1])
C3714660 (UMLS CUI [1,2])
Informed Consent Unable | Informed Consent Unwilling
Item
subjects unable or unwilling to undergo informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Medical contraindication Contrast-enhanced Magnetic Resonance Imaging
Item
absolute contraindication to cemri, including:
boolean
C1301624 (UMLS CUI [1,1])
C1707501 (UMLS CUI [1,2])
Implant Electrical | Artificial cardiac pacemaker | Neurostimulator | Aneurysm clip | Metallic foreign body Intraocular | Metallic foreign body Nearby Eye
Item
1. presence of implanted electrical device (pacemaker or neurostimulator),aneurysm clip, or metallic foreign body in or near the eyes
boolean
C0021102 (UMLS CUI [1,1])
C0442828 (UMLS CUI [1,2])
C0030163 (UMLS CUI [2])
C0582124 (UMLS CUI [3])
C0179977 (UMLS CUI [4])
C1720389 (UMLS CUI [5,1])
C3282905 (UMLS CUI [5,2])
C1720389 (UMLS CUI [6,1])
C1706276 (UMLS CUI [6,2])
C0015392 (UMLS CUI [6,3])
Hypersensitivity Life Threatening Gadolinium-based Contrast Agent
Item
2. life threatening allergy to gadolinium contrast
boolean
C0020517 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
C3249258 (UMLS CUI [1,3])
Contrast-enhanced Magnetic Resonance Imaging Performed | Exception Medical center Specified
Item
cemri performed at institution other than dhmc lebanon
boolean
C1707501 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0565990 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
Neoadjuvant Therapy
Item
patients undergoing neoadjuvant therapy
boolean
C0600558 (UMLS CUI [1])
Tumor Diameter Size Maximum
Item
patients with maximum tumor diameter >5cm
boolean
C0027651 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
C0806909 (UMLS CUI [1,4])
Inflammatory Breast Carcinoma
Item
patients presenting with inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
Axillary lymphadenopathy Gross Medical Examination | Axillary lymphadenopathy Gross Imaging
Item
patients with gross axillary lymphadenopathy on clinical exam or by imaging
boolean
C0578735 (UMLS CUI [1,1])
C0439806 (UMLS CUI [1,2])
C0582103 (UMLS CUI [1,3])
C0578735 (UMLS CUI [2,1])
C0439806 (UMLS CUI [2,2])
C0011923 (UMLS CUI [2,3])
Breast Size Maximum Limitation
Item
maximum breast size limitation: i.e. breast size that exceeds the size of the large format image receptor (24cm x 29cm) on any view
boolean
C0425782 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
C0449295 (UMLS CUI [1,3])

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