Informatie:
Fout:
ID
38118
Beschrijving
Pilot Indocyanine Green™ Imaging for Mapping of Arm Draining Lymphatics & Nodes in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01771666
Link
https://clinicaltrials.gov/show/NCT01771666
Trefwoorden
Versies (1)
- 18-09-19 18-09-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
18 september 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01771666
Eligibility Breast Cancer NCT01771666
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01771666
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Comprehension Informed Consent | Consent sign Willing
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0162340 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0742766 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
C0021430 (UMLS CUI [1,2])
C0742766 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Informed Consent
Item
signed written informed consent.
boolean
C0021430 (UMLS CUI [1])
Gender | Sentinel Lymph Node Biopsy
Item
women undergoing sentinel lymph node biopsy.
boolean
C0079399 (UMLS CUI [1])
C0796693 (UMLS CUI [2])
C0796693 (UMLS CUI [2])
Gender | Breast Carcinoma | Lymph Node Involvement | Lymph Node Involvement Suspected
Item
women with breast cancer with known or suspected lymph node involvement.
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C0806692 (UMLS CUI [3])
C0806692 (UMLS CUI [4,1])
C0750491 (UMLS CUI [4,2])
C0678222 (UMLS CUI [2])
C0806692 (UMLS CUI [3])
C0806692 (UMLS CUI [4,1])
C0750491 (UMLS CUI [4,2])
Gender | Sentinel Lymph Node Identification | Excision of axillary lymph nodes Completion
Item
women undergoing sentinel node identification and completion axillary lymph node dissection.
boolean
C0079399 (UMLS CUI [1])
C1522495 (UMLS CUI [2,1])
C0205396 (UMLS CUI [2,2])
C0193867 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C1522495 (UMLS CUI [2,1])
C0205396 (UMLS CUI [2,2])
C0193867 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
Gender | Age
Item
women of 18 years of age or older.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
ECOG performance status | Karnofsky Performance Status
Item
eastern cooperative oncology group (ecog) or karnofsky performance status 0,1,2.
boolean
C1520224 (UMLS CUI [1])
C0206065 (UMLS CUI [2])
C0206065 (UMLS CUI [2])
Complete Blood Count | Basic metabolic panel
Item
complete blood count (cbc) and basic metabolic panel within 6 months
boolean
C0009555 (UMLS CUI [1])
C2237045 (UMLS CUI [2])
C2237045 (UMLS CUI [2])
Liver Failure | Kidney Failure
Item
history of liver or kidney failure will not be eligible.
boolean
C0085605 (UMLS CUI [1])
C0035078 (UMLS CUI [2])
C0035078 (UMLS CUI [2])
Iodine allergy
Item
allergies to iodine containing products will not be eligible.
boolean
C0571818 (UMLS CUI [1])
Pregnancy
Item
women who are pregnant will not be eligible.
boolean
C0032961 (UMLS CUI [1])
Mental disorders Protocol Compliance Excluded | Addictive Behavior Protocol Compliance Excluded | Condition Protocol Compliance Excluded
Item
psychiatric or addictive disorders or other conditions that, in the opinion of the investigator, would preclude the patient from meeting the study requirements.
boolean
C0004936 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C0085281 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C0348080 (UMLS CUI [3,1])
C0525058 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C0525058 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C0085281 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C0348080 (UMLS CUI [3,1])
C0525058 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])