ID

31697

Description

The Contribution of Lp-PLA2 Level to the Presence of Coronary Plaques in Patients With Non Alcoholic Fatty Liver Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01139632

Link

https://clinicaltrials.gov/show/NCT01139632

Keywords

Versions (2)
  1. 9/21/18 9/21/18 -
  2. 9/21/18 9/21/18 - Sarah Riepenhausen
Copyright Holder

Ziv Hospital

Uploaded on

September 21, 2018

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
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.

Back to model comments
Itemgroup comments for :

Item comments for :

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

Eligibility Coronary Plaques in Nonalcoholic Fatty Liver Disease NCT01139632

English

Eligibility Nonalcoholic Fatty Liver Disease NCT01139632

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. patients at intermediate risk for significant cad was admitted to the hospital with the diagnosis of chest pain or undergoing elective ct coronarography due to suspection of coronary artery disease.
Description

intermediate risk patients for having significant cad is defined as: - chest pain or dyspnea in the presence of negative stress tests - the absence of chest pain but positive stress tests - the absence of chest pain and of positive stress tests but intermittent arrhythmias

Data type

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C3275094
UMLS CUI [2,1]
C1956346
UMLS CUI [2,2]
C0332147
UMLS CUI [3,1]
C0184666
UMLS CUI [3,2]
C0008031
UMLS CUI [4]
C0085532
2. male and female 18years or older.
Description

Age and Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
3. able to provide written informed consent.
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. acute coronary syndrome presentation:
Description

acute coronary syndrome presentation

Data type

boolean

Alias
UMLS CUI [1]
C0948089
st segment deviation on ecg and/or
Description

St segment deviation on ecg

Data type

boolean

Alias
UMLS CUI [1]
C1116089
2. cardiac troponin elevation.
Description

Cardiac troponin elevation

Data type

boolean

Alias
UMLS CUI [1]
C0523952
3. chest pain in combination with positive tests for myocardial ischemia
Description

Chest pain in combination with positive test for myocardial ischemia

Data type

boolean

Alias
UMLS CUI [1,1]
C0008031
UMLS CUI [1,2]
C0151744
UMLS CUI [1,3]
C2711652
4. hemodynamic instability on presentation.
Description

Hemodynamic instability

Data type

boolean

Alias
UMLS CUI [1]
C0948268
5. inability to write inform consent.
Description

Inability to informed consent

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
6. age <18 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
7. participation in an investigational study within the previous 30days.
Description

Recent participation in an investigational study

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0332185
Back to the top of the page

Similar models

Eligibility Nonalcoholic Fatty Liver Disease NCT01139632

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
patients at intermediate risk for significant cad and chest pain
Item
1. patients at intermediate risk for significant cad was admitted to the hospital with the diagnosis of chest pain or undergoing elective ct coronarography due to suspection of coronary artery disease.
boolean
C1956346 (UMLS CUI [1,1])
C3275094 (UMLS CUI [1,2])
C1956346 (UMLS CUI [2,1])
C0332147 (UMLS CUI [2,2])
C0184666 (UMLS CUI [3,1])
C0008031 (UMLS CUI [3,2])
C0085532 (UMLS CUI [4])
Age and Gender
Item
2. male and female 18years or older.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Informed consent
Item
3. able to provide written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
acute coronary syndrome presentation
Item
1. acute coronary syndrome presentation:
boolean
C0948089 (UMLS CUI [1])
St segment deviation on ecg
Item
st segment deviation on ecg and/or
boolean
C1116089 (UMLS CUI [1])
Cardiac troponin elevation
Item
2. cardiac troponin elevation.
boolean
C0523952 (UMLS CUI [1])
Chest pain in combination with positive test for myocardial ischemia
Item
3. chest pain in combination with positive tests for myocardial ischemia
boolean
C0008031 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
C2711652 (UMLS CUI [1,3])
Hemodynamic instability
Item
4. hemodynamic instability on presentation.
boolean
C0948268 (UMLS CUI [1])
Inability to informed consent
Item
5. inability to write inform consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Age
Item
6. age <18 years.
boolean
C0001779 (UMLS CUI [1])
Recent participation in an investigational study
Item
7. participation in an investigational study within the previous 30days.
boolean
C2348568 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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