ID

24463

Description

Resynchronization Surgery Combined Unified Efficacy; ODM derived from: https://clinicaltrials.gov/show/NCT00846001

Link

https://clinicaltrials.gov/show/NCT00846001

Keywords

Versions (1)
  1. 8/2/17 8/2/17 -
Uploaded on

August 2, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Ischemic Heart Failure NCT00846001

English

Eligibility Ischemic Heart Failure NCT00846001

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
men and women
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
age 18-80
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
history of ischemic heart failure and indications for cabg
Description

Heart failure Ischemic | Indication for Coronary Artery Bypass Surgery

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0475224
UMLS CUI [2,1]
C0392360
UMLS CUI [2,2]
C0010055
lvef less than 35% estimated by echocardiography measured within 3 months of study entry
Description

Left ventricular ejection fraction Echocardiography

Data type

boolean

Alias
UMLS CUI [1,1]
C0428772
UMLS CUI [1,2]
C0013516
nyha and ccs (angina) ii-iv functional class
Description

New York Heart Association Classification | Canadian Cardiovascular Society Grading Scale Class

Data type

boolean

Alias
UMLS CUI [1]
C1275491
UMLS CUI [2]
C1879987
signs of dyssynchrony (at least one of the following three): qrs > 120 ms or dyssynchrony based on doppler-methods (tissue tracking and tsi methods) or care hf criteria: aortic pre-ejection delay >140ms, interventricular mechanical delay >40 ms, delayed activation of postero-lateral lv wall
Description

Ventricular dyssynchrony Signs | QRS complex duration | Ventricular dyssynchrony Doppler ultrasonography of heart tissue | Care Heart failure Criteria | Pre-ejection period of aortic valve Delay | Interventricular dyssynchrony | Left ventricular wall motion Posterolateral Delayed

Data type

boolean

Alias
UMLS CUI [1,1]
C3160931
UMLS CUI [1,2]
C0311392
UMLS CUI [2]
C0429025
UMLS CUI [3,1]
C3160931
UMLS CUI [3,2]
C2585212
UMLS CUI [4,1]
C1947933
UMLS CUI [4,2]
C0018801
UMLS CUI [4,3]
C0243161
UMLS CUI [5,1]
C2059412
UMLS CUI [5,2]
C0205421
UMLS CUI [6]
C3531870
UMLS CUI [7,1]
C0455816
UMLS CUI [7,2]
C0332195
UMLS CUI [7,3]
C0205421
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
failure to provide informed consent.
Description

Informed Consent Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
previous cardiac surgery
Description

Cardiac Surgery procedures

Data type

boolean

Alias
UMLS CUI [1]
C0018821
non-cardiac illness with a life expectancy of less than 3 year
Description

Illness | Heart Diseases Excluded | Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0221423
UMLS CUI [2,1]
C0018799
UMLS CUI [2,2]
C2828389
UMLS CUI [3]
C0023671
non-cardiac illness imposing substantial operative mortality
Description

Illness Relationship Mortality Operative | Heart Diseases Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0439849
UMLS CUI [1,3]
C0026566
UMLS CUI [1,4]
C1882154
UMLS CUI [2,1]
C0018799
UMLS CUI [2,2]
C2828389
previous heart, kidney, liver, or lung transplantation
Description

Heart Transplantation | Kidney Transplantation | Transplantation of liver | Lung Transplantation

Data type

boolean

Alias
UMLS CUI [1]
C0018823
UMLS CUI [2]
C0022671
UMLS CUI [3]
C0023911
UMLS CUI [4]
C0024128
current participation in another clinical trial in which a patient is taking an investigational drug or receiving an investigational medical device
Description

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
successful coronary revascularization (сabg or pci) within 12 months of study enrollment
Description

Coronary revascularisation Successful | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Data type

boolean

Alias
UMLS CUI [1,1]
C0877341
UMLS CUI [1,2]
C1272703
UMLS CUI [2]
C0010055
UMLS CUI [3]
C1532338
chronic atrial fibrillation
Description

Chronic atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C0694539
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Similar models

Eligibility Ischemic Heart Failure NCT00846001

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
men and women
boolean
C0079399 (UMLS CUI [1])
Age
Item
age 18-80
boolean
C0001779 (UMLS CUI [1])
Heart failure Ischemic | Indication for Coronary Artery Bypass Surgery
Item
history of ischemic heart failure and indications for cabg
boolean
C0018801 (UMLS CUI [1,1])
C0475224 (UMLS CUI [1,2])
C0392360 (UMLS CUI [2,1])
C0010055 (UMLS CUI [2,2])
Left ventricular ejection fraction Echocardiography
Item
lvef less than 35% estimated by echocardiography measured within 3 months of study entry
boolean
C0428772 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
New York Heart Association Classification | Canadian Cardiovascular Society Grading Scale Class
Item
nyha and ccs (angina) ii-iv functional class
boolean
C1275491 (UMLS CUI [1])
C1879987 (UMLS CUI [2])
Ventricular dyssynchrony Signs | QRS complex duration | Ventricular dyssynchrony Doppler ultrasonography of heart tissue | Care Heart failure Criteria | Pre-ejection period of aortic valve Delay | Interventricular dyssynchrony | Left ventricular wall motion Posterolateral Delayed
Item
signs of dyssynchrony (at least one of the following three): qrs > 120 ms or dyssynchrony based on doppler-methods (tissue tracking and tsi methods) or care hf criteria: aortic pre-ejection delay >140ms, interventricular mechanical delay >40 ms, delayed activation of postero-lateral lv wall
boolean
C3160931 (UMLS CUI [1,1])
C0311392 (UMLS CUI [1,2])
C0429025 (UMLS CUI [2])
C3160931 (UMLS CUI [3,1])
C2585212 (UMLS CUI [3,2])
C1947933 (UMLS CUI [4,1])
C0018801 (UMLS CUI [4,2])
C0243161 (UMLS CUI [4,3])
C2059412 (UMLS CUI [5,1])
C0205421 (UMLS CUI [5,2])
C3531870 (UMLS CUI [6])
C0455816 (UMLS CUI [7,1])
C0332195 (UMLS CUI [7,2])
C0205421 (UMLS CUI [7,3])
Item Group
C0680251 (UMLS CUI)
Informed Consent Lacking
Item
failure to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Cardiac Surgery procedures
Item
previous cardiac surgery
boolean
C0018821 (UMLS CUI [1])
Illness | Heart Diseases Excluded | Life Expectancy
Item
non-cardiac illness with a life expectancy of less than 3 year
boolean
C0221423 (UMLS CUI [1])
C0018799 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
Illness Relationship Mortality Operative | Heart Diseases Excluded
Item
non-cardiac illness imposing substantial operative mortality
boolean
C0221423 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C0026566 (UMLS CUI [1,3])
C1882154 (UMLS CUI [1,4])
C0018799 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Heart Transplantation | Kidney Transplantation | Transplantation of liver | Lung Transplantation
Item
previous heart, kidney, liver, or lung transplantation
boolean
C0018823 (UMLS CUI [1])
C0022671 (UMLS CUI [2])
C0023911 (UMLS CUI [3])
C0024128 (UMLS CUI [4])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
current participation in another clinical trial in which a patient is taking an investigational drug or receiving an investigational medical device
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Coronary revascularisation Successful | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
successful coronary revascularization (сabg or pci) within 12 months of study enrollment
boolean
C0877341 (UMLS CUI [1,1])
C1272703 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
Chronic atrial fibrillation
Item
chronic atrial fibrillation
boolean
C0694539 (UMLS CUI [1])
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