Information:
Error:
ID
28587
Description
Alternative in Beta Blocker Intolerance: The ABBI Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00893984
Link
https://clinicaltrials.gov/show/NCT00893984
Keywords
Versions (1)
- 1/23/18 1/23/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
January 23, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00893984
Eligibility Coronary Artery Disease NCT00893984
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT00893984
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Age
Item
age ≥ 21
boolean
C0001779 (UMLS CUI [1])
Gender | Postmenopausal state | Pregnancy Absent | Contraceptive methods
Item
male or female who is post-menopausal or not pregnant and using an approved contraceptive regimen
boolean
C0079399 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0700589 (UMLS CUI [4])
C0232970 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0700589 (UMLS CUI [4])
Adrenergic beta-Antagonists Previous | Intolerance to Adrenergic beta-Antagonists
Item
previous beta blocker use and intolerant of beta blocker
boolean
C0001645 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0001645 (UMLS CUI [2,2])
C0205156 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0001645 (UMLS CUI [2,2])
Systolic Pressure | Exception Antihypertensive Agent Discontinued
Item
systolic blood pressure < 100 mmhg unless another blood pressure medication is stopped at the time of study entry
boolean
C0871470 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0003364 (UMLS CUI [2,2])
C1444662 (UMLS CUI [2,3])
C1705847 (UMLS CUI [2,1])
C0003364 (UMLS CUI [2,2])
C1444662 (UMLS CUI [2,3])
Hospitalization Due to Heart Failure
Item
hospitalized for heart failure within the past 4 weeks
boolean
C3898876 (UMLS CUI [1])
Bradycardia | Heart rate
Item
bradycardia with a heart rate < 60
boolean
C0428977 (UMLS CUI [1])
C0018810 (UMLS CUI [2])
C0018810 (UMLS CUI [2])
Second degree atrioventricular block | Complete atrioventricular block
Item
heart block greater than first degree
boolean
C0264906 (UMLS CUI [1])
C0151517 (UMLS CUI [2])
C0151517 (UMLS CUI [2])
Sick Sinus Syndrome | Exception Permanent pacemaker insertion
Item
history of sick sinus syndrome (unless a permanent pacemaker is in place)
boolean
C0037052 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C2924511 (UMLS CUI [2,2])
C1705847 (UMLS CUI [2,1])
C2924511 (UMLS CUI [2,2])
Liver Dysfunction Severe | Renal dysfunction Severe | Serum creatinine raised | Serum amylase raised
Item
history of severe hepatic or renal dysfunction; serum creatinine > 2.0 or amylase > 3x normal
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3279454 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0700225 (UMLS CUI [3])
C0476327 (UMLS CUI [4])
C0205082 (UMLS CUI [1,2])
C3279454 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0700225 (UMLS CUI [3])
C0476327 (UMLS CUI [4])
CYP2D6 Inhibitors | Quinidine | Propafenone | Fluoxetine | Paroxetine
Item
use of cyp2d6 inhibitors (quinidine, propafenone, fluoxetine, paroxetine, etc.)
boolean
C3850058 (UMLS CUI [1])
C0034414 (UMLS CUI [2])
C0033429 (UMLS CUI [3])
C0016365 (UMLS CUI [4])
C0070122 (UMLS CUI [5])
C0034414 (UMLS CUI [2])
C0033429 (UMLS CUI [3])
C0016365 (UMLS CUI [4])
C0070122 (UMLS CUI [5])
Investigational New Drugs
Item
ingestion of investigational drug within the past 30 days
boolean
C0013230 (UMLS CUI [1])