Informatie:
Fout:
ID
33899
Beschrijving
Pilot Study of Bone Biopsy and Aspirate in Women With Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01975597
Link
https://clinicaltrials.gov/show/NCT01975597
Trefwoorden
Versies (1)
- 06-01-19 06-01-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
6 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Metastatic Breast Cancer NCT01975597
Eligibility Metastatic Breast Cancer NCT01975597
- StudyEvent: Eligibility
Similar models
Eligibility Metastatic Breast Cancer NCT01975597
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Secondary malignant neoplasm of female breast | Age
Item
patients with metastatic breast cancer (any site) age 21 or older
boolean
C0346993 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Informed Consent | Protocol Compliance
Item
patients willing and able to provide informed consent & perform study procedures
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
C0525058 (UMLS CUI [2])
Tumor Burden Stable | Tumor Burden Response | Tumor Burden Progressive
Item
patients may enroll with stable, responding or progressive tumor burden
boolean
C1449699 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C1449699 (UMLS CUI [2,1])
C1704632 (UMLS CUI [2,2])
C1449699 (UMLS CUI [3,1])
C0205329 (UMLS CUI [3,2])
C0205360 (UMLS CUI [1,2])
C1449699 (UMLS CUI [2,1])
C1704632 (UMLS CUI [2,2])
C1449699 (UMLS CUI [3,1])
C0205329 (UMLS CUI [3,2])
Performance status
Item
performance status of 0,1 or 2
boolean
C1518965 (UMLS CUI [1])
Informed Consent Unable | Informed Consent Unwilling | Protocol Compliance Unable | Protocol Compliance Unwilling
Item
patients unable or unwilling to provide informed consent and or perform study procedures
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C0525058 (UMLS CUI [4,1])
C0558080 (UMLS CUI [4,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C0525058 (UMLS CUI [4,1])
C0558080 (UMLS CUI [4,2])
Blood Coagulation Disorder Uncontrolled
Item
patients with active, uncontrolled coagulopathy
boolean
C0005779 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,2])
Anticoagulation Therapy Dose | International Normalized Ratio | Relationship Warfarin
Item
patients on treatment dose anticoagulation or an international normalised ratio of 2 or greater if on warfarin
boolean
C0003281 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0525032 (UMLS CUI [2])
C0439849 (UMLS CUI [3,1])
C0043031 (UMLS CUI [3,2])
C0178602 (UMLS CUI [1,2])
C0525032 (UMLS CUI [2])
C0439849 (UMLS CUI [3,1])
C0043031 (UMLS CUI [3,2])
Pregnancy
Item
patients who are known to be pregnant are not eligible to participate in this study during the time of the pregnancy
boolean
C0032961 (UMLS CUI [1])