ID

24718

Description

Endocardial Stem Cells Approach Efficacy; ODM derived from: https://clinicaltrials.gov/show/NCT00841958

Link

https://clinicaltrials.gov/show/NCT00841958

Keywords

  1. 8/14/17 8/14/17 -
Uploaded on

August 14, 2017

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :


No comments

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Myocardial Ischemia NCT00841958

Eligibility Myocardial Ischemia NCT00841958

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
men and women who are not of childbearing potential
Description

Childbearing Potential Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0332197
age 21-75 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients with cad, nyha and ccs angina iii-iv functional class
Description

Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Angina Pectoris Canadian Cardiovascular Society classification

Data type

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2,1]
C0002962
UMLS CUI [2,2]
C1275491
UMLS CUI [3,1]
C0002962
UMLS CUI [3,2]
C1277207
lvef less than 35% measured by echocardiography or spect within three months of study entry
Description

Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction SPECT

Data type

boolean

Alias
UMLS CUI [1,1]
C0428772
UMLS CUI [1,2]
C0013516
UMLS CUI [2,1]
C0428772
UMLS CUI [2,2]
C0040399
unsuitable for initial or repeated conventional revascularization (cabg or pci)
Description

Inappropriate Revascularization Initial | Inappropriate Revascularization Repeated | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Data type

boolean

Alias
UMLS CUI [1,1]
C1548788
UMLS CUI [1,2]
C0581603
UMLS CUI [1,3]
C0205265
UMLS CUI [2,1]
C1548788
UMLS CUI [2,2]
C0581603
UMLS CUI [2,3]
C0205341
UMLS CUI [3]
C0010055
UMLS CUI [4]
C1532338
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
plan for pci or cabg.
Description

Percutaneous Coronary Intervention Planned | Coronary Artery Bypass Surgery Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0010055
UMLS CUI [2,2]
C1301732
non-cardiac illness with a life expectancy of less than 3 year.
Description

Illness | Exception Heart Diseases | Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0221423
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018799
UMLS CUI [3]
C0023671
conditions/circumstances likely to lead to poor treatment adherence (e.g., history of poor compliance, alcohol or drug dependency, psychiatric illness, no fixed abode).
Description

Condition Adherence to treatment plan Poor | Compliance behavior Poor | Substance Dependence | Mental disorders | No fixed abode

Data type

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0516958
UMLS CUI [1,3]
C0542537
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0542537
UMLS CUI [3]
C0038580
UMLS CUI [4]
C0004936
UMLS CUI [5]
C0557219
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
recent acute myocardial infarction (ami) within 90 days of study entry
Description

Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
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
history of moderate to severe aortic stenosis or prosthetic aortic valve
Description

Aortic Valve Stenosis Moderate | Aortic stenosis, severe | Aortic valve prosthesis

Data type

boolean

Alias
UMLS CUI [1,1]
C0003507
UMLS CUI [1,2]
C0205081
UMLS CUI [2]
C3806272
UMLS CUI [3]
C0182431
permanent atrial fibrillation
Description

Permanent atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C2586056
thrombosis in lv, based on echocardiography data
Description

Left ventricular thrombosis Echocardiography

Data type

boolean

Alias
UMLS CUI [1,1]
C0587044
UMLS CUI [1,2]
C0013516

Similar models

Eligibility Myocardial Ischemia NCT00841958

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Childbearing Potential Absent
Item
men and women who are not of childbearing potential
boolean
C3831118 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Age
Item
age 21-75 years.
boolean
C0001779 (UMLS CUI [1])
Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Angina Pectoris Canadian Cardiovascular Society classification
Item
patients with cad, nyha and ccs angina iii-iv functional class
boolean
C1956346 (UMLS CUI [1])
C0002962 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
C0002962 (UMLS CUI [3,1])
C1277207 (UMLS CUI [3,2])
Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction SPECT
Item
lvef less than 35% measured by echocardiography or spect within three months of study entry
boolean
C0428772 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0428772 (UMLS CUI [2,1])
C0040399 (UMLS CUI [2,2])
Inappropriate Revascularization Initial | Inappropriate Revascularization Repeated | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
unsuitable for initial or repeated conventional revascularization (cabg or pci)
boolean
C1548788 (UMLS CUI [1,1])
C0581603 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
C1548788 (UMLS CUI [2,1])
C0581603 (UMLS CUI [2,2])
C0205341 (UMLS CUI [2,3])
C0010055 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
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])
Percutaneous Coronary Intervention Planned | Coronary Artery Bypass Surgery Planned
Item
plan for pci or cabg.
boolean
C1532338 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Illness | Exception Heart Diseases | Life Expectancy
Item
non-cardiac illness with a life expectancy of less than 3 year.
boolean
C0221423 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
Condition Adherence to treatment plan Poor | Compliance behavior Poor | Substance Dependence | Mental disorders | No fixed abode
Item
conditions/circumstances likely to lead to poor treatment adherence (e.g., history of poor compliance, alcohol or drug dependency, psychiatric illness, no fixed abode).
boolean
C0348080 (UMLS CUI [1,1])
C0516958 (UMLS CUI [1,2])
C0542537 (UMLS CUI [1,3])
C1321605 (UMLS CUI [2,1])
C0542537 (UMLS CUI [2,2])
C0038580 (UMLS CUI [3])
C0004936 (UMLS CUI [4])
C0557219 (UMLS CUI [5])
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])
Myocardial Infarction
Item
recent acute myocardial infarction (ami) within 90 days of study entry
boolean
C0027051 (UMLS CUI [1])
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])
Aortic Valve Stenosis Moderate | Aortic stenosis, severe | Aortic valve prosthesis
Item
history of moderate to severe aortic stenosis or prosthetic aortic valve
boolean
C0003507 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C3806272 (UMLS CUI [2])
C0182431 (UMLS CUI [3])
Permanent atrial fibrillation
Item
permanent atrial fibrillation
boolean
C2586056 (UMLS CUI [1])
Left ventricular thrombosis Echocardiography
Item
thrombosis in lv, based on echocardiography data
boolean
C0587044 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial