Informatie:
Fout:
ID
26086
Beschrijving
Neoadjuvant Endostatin and Chemotherapy for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00604435
Link
https://clinicaltrials.gov/show/NCT00604435
Trefwoorden
Versies (1)
- 09-10-17 09-10-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
9 oktober 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Breast Cancer NCT00604435
Eligibility Breast Cancer NCT00604435
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00604435
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Invasive carcinoma of breast | Core needle biopsy Breast Carcinoma | Fine needle aspiration Secondary malignant neoplasm of lymph node
Item
histologically confirmed invasive breast cancer (core needle biopsy for breast cancer diagnosis and fine needle aspiration for lymph node metastasis diagnosis)
boolean
C0853879 (UMLS CUI [1])
C1318309 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1510483 (UMLS CUI [3,1])
C0686619 (UMLS CUI [3,2])
C1318309 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1510483 (UMLS CUI [3,1])
C0686619 (UMLS CUI [3,2])
TNM clinical staging
Item
stage ⅱa-ⅲc
boolean
C3258246 (UMLS CUI [1])
Age
Item
age 18-70
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Distant metastasis Absent
Item
no evidence of distant metastasis
boolean
C1269798 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Prior Therapy Absent
Item
no previous therapy
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Hematologic function
Item
normal hematologic function
boolean
C0221130 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction greater than 50 percent
boolean
C0428772 (UMLS CUI [1])
Renal function | Liver function
Item
no abnormality of renal or liver function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232741 (UMLS CUI [2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Allergic disposition | Allergic Reaction Investigational New Drugs
Item
with allergic constitution or possible allergic reflection to drugs to be used in this study
boolean
C3539909 (UMLS CUI [1])
C1527304 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C1527304 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Disease Uncontrolled | Mental disorder Uncontrolled
Item
any concurrent uncontrolled medical or psychiatric disorder
boolean
C0012634 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0004936 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0205318 (UMLS CUI [1,2])
C0004936 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
Heart Diseases Severe | Congestive heart failure | Angina, Unstable | Cardiac Arrhythmia Uncontrolled | Myocardial Infarction | Uncontrolled hypertension | Heart valve disease
Item
history of severe heart diseases, including congestive heart failure, unstable angina, uncontrolled arrhythmia, myocardial infarction, uncontrolled high blood pressure, or heart valve disease.
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0003811 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
C0027051 (UMLS CUI [5])
C1868885 (UMLS CUI [6])
C0018824 (UMLS CUI [7])
C0205082 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0003811 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
C0027051 (UMLS CUI [5])
C1868885 (UMLS CUI [6])
C0018824 (UMLS CUI [7])
Bleeding tendency
Item
history of bleeding diathesis
boolean
C1458140 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
being pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])