Informatie:
Fout:
ID
38131
Beschrijving
FACBC PET and PEM as a Staging Tool and Indicator of Therapeutic Response in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01864083
Link
https://clinicaltrials.gov/show/NCT01864083
Trefwoorden
Versies (1)
- 20-09-19 20-09-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
20 september 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01864083
Eligibility Breast Cancer NCT01864083
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01864083
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Gender | Invasive Ductal Breast Carcinoma Biopsy | Invasive Lobular Breast Carcinoma Biopsy
Item
women presenting for evaluation at mskcc with biopsy proven primary idc or ilc
boolean
C0079399 (UMLS CUI [1])
C1134719 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C0279565 (UMLS CUI [3,1])
C0005558 (UMLS CUI [3,2])
C1134719 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C0279565 (UMLS CUI [3,1])
C0005558 (UMLS CUI [3,2])
Prior Therapy Absent Invasive Ductal Breast Carcinoma | Prior Therapy Absent Invasive Lobular Breast Carcinoma
Item
no prior therapy for idc or ilc
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1134719 (UMLS CUI [1,3])
C1514463 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0279565 (UMLS CUI [2,3])
C0332197 (UMLS CUI [1,2])
C1134719 (UMLS CUI [1,3])
C1514463 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0279565 (UMLS CUI [2,3])
Local disease TNM Breast tumor staging | Magnetic resonance imaging of breast
Item
clinical need for local disease staging with breast mr (group a only)
boolean
C0277565 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
C0344104 (UMLS CUI [2])
C0474926 (UMLS CUI [1,2])
C0344104 (UMLS CUI [2])
Patient need for Neoadjuvant Chemotherapy
Item
clinical need for neoadjuvant chemotherapy (group b only)
boolean
C0686904 (UMLS CUI [1,1])
C0600558 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,3])
C0600558 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,3])
Informed Consent
Item
patients must provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age <21 years
boolean
C0001779 (UMLS CUI [1])
Gender
Item
men
boolean
C0079399 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Therapeutic procedure Started Malignant Neoplasms
Item
patients who have already started treatment for the current malignancy
boolean
C0087111 (UMLS CUI [1,1])
C1272689 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C1272689 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
PET scan Unsuccessful | Etiology Body Weight Limit
Item
patients who cannot undergo pet scanning (i.e. because of weight limits)
boolean
C0032743 (UMLS CUI [1,1])
C1272705 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0005910 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
C1272705 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0005910 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
Medical contraindication MRI | Presence of metallic implant
Item
patients who are known to have contraindication for mri (e.g. metal implants)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C3693688 (UMLS CUI [2])
C0024485 (UMLS CUI [1,2])
C3693688 (UMLS CUI [2])
Study Subject Participation Status | Group Singular
Item
patients may only participate in group #1 or group #2, but not both
boolean
C2348568 (UMLS CUI [1])
C0441833 (UMLS CUI [2,1])
C0205171 (UMLS CUI [2,2])
C0441833 (UMLS CUI [2,1])
C0205171 (UMLS CUI [2,2])