ID

30147

Description

Revascularization in Heart Failure Trial – REHEAT 2; ODM derived from: https://clinicaltrials.gov/show/NCT00388245

Link

https://clinicaltrials.gov/show/NCT00388245

Keywords

Versions (1)
  1. 5/15/18 5/15/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 15, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Left Ventricular Ejection Fraction NCT00388245

English

Eligibility Left Ventricular Ejection Fraction NCT00388245

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic coronary artery disease (angina ccs class 1)
Description

Coronary Artery Disease Symptomatic CCS Class

Data type

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C1879987
left ventricle ejection fraction <40%
Description

Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0428772
coronary artery lesions suitable for percutaneous or surgical myocardial revascularisation
Description

Coronary artery Lesion Appropriate Percutaneous Coronary Revascularization | Coronary artery Lesion Appropriate Myocardial Revascularization

Data type

boolean

Alias
UMLS CUI [1,1]
C0205042
UMLS CUI [1,2]
C0221198
UMLS CUI [1,3]
C1548787
UMLS CUI [1,4]
C1532338
UMLS CUI [2,1]
C0205042
UMLS CUI [2,2]
C0221198
UMLS CUI [2,3]
C1548787
UMLS CUI [2,4]
C0027056
evidence for viability of the myocardium
Description

Myocardium Viable

Data type

boolean

Alias
UMLS CUI [1,1]
C0027061
UMLS CUI [1,2]
C0443348
written inform consent for the study
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age <18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
acute myocardial infarct with st elevation within 30 days
Description

ST segment elevation myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C1536220
concomitant congenital heart disease
Description

Congenital heart disease

Data type

boolean

Alias
UMLS CUI [1]
C0152021
mitral regurgitation required surgical intervention
Description

Mitral Valve Insufficiency Requirement Surgical intervention

Data type

boolean

Alias
UMLS CUI [1,1]
C0026266
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C4035998
history of bleeding diathesis, coagulopathy or abnormal bleeding within the previous 30 days.
Description

Bleeding tendency | Blood Coagulation Disorder

Data type

boolean

Alias
UMLS CUI [1]
C1458140
UMLS CUI [2]
C0005779
major surgery within the previous 6 weeks
Description

Major surgery

Data type

boolean

Alias
UMLS CUI [1]
C0679637
stroke or transient ischemic attack (tia) within the previous 6 weeks
Description

Cerebrovascular accident | Transient Ischemic Attack

Data type

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
history of hemorrhagic stroke
Description

Brain hemorrhage

Data type

boolean

Alias
UMLS CUI [1]
C0553692
uncontrolled hypertension
Description

Uncontrolled hypertension

Data type

boolean

Alias
UMLS CUI [1]
C1868885
chronic renal insufficiency with creatinine >2.0 mg/dl
Description

Chronic Kidney Insufficiency | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0403447
UMLS CUI [2]
C0201976
platelet count <100.000/mm3
Description

Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C0032181
hematocrit <30%
Description

Hematocrit procedure

Data type

boolean

Alias
UMLS CUI [1]
C0018935
pt >1,2 times control
Description

Prothrombin time increased

Data type

boolean

Alias
UMLS CUI [1]
C0151872
positive pregnancy test
Description

Pregnancy test positive

Data type

boolean

Alias
UMLS CUI [1]
C0240802
any disease that may shorten the life expectancy of the patient
Description

Disease Limiting Life Expectancy

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0023671
the patient is currently participating in another research study
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Left Ventricular Ejection Fraction NCT00388245

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Coronary Artery Disease Symptomatic CCS Class
Item
symptomatic coronary artery disease (angina ccs class 1)
boolean
C1956346 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C1879987 (UMLS CUI [1,3])
Left ventricular ejection fraction
Item
left ventricle ejection fraction <40%
boolean
C0428772 (UMLS CUI [1])
Coronary artery Lesion Appropriate Percutaneous Coronary Revascularization | Coronary artery Lesion Appropriate Myocardial Revascularization
Item
coronary artery lesions suitable for percutaneous or surgical myocardial revascularisation
boolean
C0205042 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1548787 (UMLS CUI [1,3])
C1532338 (UMLS CUI [1,4])
C0205042 (UMLS CUI [2,1])
C0221198 (UMLS CUI [2,2])
C1548787 (UMLS CUI [2,3])
C0027056 (UMLS CUI [2,4])
Myocardium Viable
Item
evidence for viability of the myocardium
boolean
C0027061 (UMLS CUI [1,1])
C0443348 (UMLS CUI [1,2])
Informed Consent
Item
written inform consent for the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
age <18 years
boolean
C0001779 (UMLS CUI [1])
ST segment elevation myocardial infarction
Item
acute myocardial infarct with st elevation within 30 days
boolean
C1536220 (UMLS CUI [1])
Congenital heart disease
Item
concomitant congenital heart disease
boolean
C0152021 (UMLS CUI [1])
Mitral Valve Insufficiency Requirement Surgical intervention
Item
mitral regurgitation required surgical intervention
boolean
C0026266 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C4035998 (UMLS CUI [1,3])
Bleeding tendency | Blood Coagulation Disorder
Item
history of bleeding diathesis, coagulopathy or abnormal bleeding within the previous 30 days.
boolean
C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
Major surgery
Item
major surgery within the previous 6 weeks
boolean
C0679637 (UMLS CUI [1])
Cerebrovascular accident | Transient Ischemic Attack
Item
stroke or transient ischemic attack (tia) within the previous 6 weeks
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Brain hemorrhage
Item
history of hemorrhagic stroke
boolean
C0553692 (UMLS CUI [1])
Uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
Chronic Kidney Insufficiency | Creatinine measurement, serum
Item
chronic renal insufficiency with creatinine >2.0 mg/dl
boolean
C0403447 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Platelet Count measurement
Item
platelet count <100.000/mm3
boolean
C0032181 (UMLS CUI [1])
Hematocrit procedure
Item
hematocrit <30%
boolean
C0018935 (UMLS CUI [1])
Prothrombin time increased
Item
pt >1,2 times control
boolean
C0151872 (UMLS CUI [1])
Pregnancy test positive
Item
positive pregnancy test
boolean
C0240802 (UMLS CUI [1])
Disease Limiting Life Expectancy
Item
any disease that may shorten the life expectancy of the patient
boolean
C0012634 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
Study Subject Participation Status
Item
the patient is currently participating in another research study
boolean
C2348568 (UMLS CUI [1])
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