Informações:
Falhas:
ID
38005
Descrição
Prevention of Cardiac Dysfunction During Adjuvant Breast Cancer Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01434134
Link
https://clinicaltrials.gov/show/NCT01434134
Palavras-chave
Versões (1)
- 07/09/2019 07/09/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
7 de setembro de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01434134
Eligibility Breast Cancer NCT01434134
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01434134
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Gender | Age
Item
women aged 18-70 years
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status 0-1
boolean
C1520224 (UMLS CUI [1])
Creatinine measurement, serum | Creatinine clearance Estimated MDRD
Item
serum creatinine < 140 μmol/l or estimated creatinine clearance > 60 ml/min (using the modification of diet and renal disease (mdrd) formula)
boolean
C0201976 (UMLS CUI [1])
C0812399 (UMLS CUI [2,1])
C0750572 (UMLS CUI [2,2])
C3839656 (UMLS CUI [2,3])
C0812399 (UMLS CUI [2,1])
C0750572 (UMLS CUI [2,2])
C3839656 (UMLS CUI [2,3])
Systolic Pressure
Item
systolic blood pressure >= 110 mghg and < 170 mmhg
boolean
C0871470 (UMLS CUI [1])
Left ventricular ejection fraction
Item
lvef >= 50%
boolean
C0428772 (UMLS CUI [1])
Hypotension | Systolic Pressure
Item
hypotension, defined as systolic blood pressure < 110 mmhg
boolean
C0020649 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0871470 (UMLS CUI [2])
Bradycardia | Heart rate
Item
bradycardia, defined as heart rate < 50 b.p.m.
boolean
C0428977 (UMLS CUI [1])
C0018810 (UMLS CUI [2])
C0018810 (UMLS CUI [2])
Anthracycline Chemotherapy Regimen
Item
prior anthracycline chemotherapy regimen
boolean
C0282564 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,2])
Malignant Neoplasms Requirement Chemotherapy | Malignant Neoplasms Requirement Therapeutic radiology procedure
Item
prior malignancy requiring chemotherapy or radiotherapy
boolean
C0006826 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
Heart failure Symptomatic
Item
symptomatic heart failure
boolean
C0018801 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,2])
Systolic dysfunction | Left ventricular ejection fraction
Item
systolic dysfunction (lvef < 50%)
boolean
C0749225 (UMLS CUI [1])
C0428772 (UMLS CUI [2])
C0428772 (UMLS CUI [2])
Coronary Artery Disease | Heart valve disease | Cardiac Arrhythmia | Conduction delay
Item
clinically significant coronary artery disease, valvular heart disease, significant arrhythmias, or conduction delays.
boolean
C1956346 (UMLS CUI [1])
C0018824 (UMLS CUI [2])
C0003811 (UMLS CUI [3])
C1398354 (UMLS CUI [4])
C0018824 (UMLS CUI [2])
C0003811 (UMLS CUI [3])
C1398354 (UMLS CUI [4])
Uncontrolled hypertension | Systolic Pressure
Item
uncontrolled arterial hypertension defined as systolic blood pressure > 170 mm hg
boolean
C1868885 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0871470 (UMLS CUI [2])
Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist | Adrenergic beta-1 Receptor Antagonists
Item
treatment with acei, arb or beta-blocker within the last 4 weeks prior to study start
boolean
C0003015 (UMLS CUI [1])
C0521942 (UMLS CUI [2])
C0304516 (UMLS CUI [3])
C0521942 (UMLS CUI [2])
C0304516 (UMLS CUI [3])
Intolerance to Angiotensin-Converting Enzyme Inhibitors | Intolerance to Angiotensin II receptor antagonist | Intolerance to Adrenergic beta-1 Receptor Antagonists
Item
intolerance to acei, arb or beta-blocker
boolean
C1744706 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0521942 (UMLS CUI [2,2])
C1744706 (UMLS CUI [3,1])
C0304516 (UMLS CUI [3,2])
C0003015 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0521942 (UMLS CUI [2,2])
C1744706 (UMLS CUI [3,1])
C0304516 (UMLS CUI [3,2])
Comorbidity Serious Uncontrolled
Item
uncontrolled concomitant serious illness
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,3])
C0205404 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Substance Use Disorders
Item
active abuse of drugs or alcohol
boolean
C0038586 (UMLS CUI [1])
Poor compliance Suspected
Item
suspected poor compliance
boolean
C0032646 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0750491 (UMLS CUI [1,2])
MRI scan Receive Unable
Item
inability to tolerate the mri scanning protocol
boolean
C0024485 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])