ID

20489

Description

The Effects of Traditional Acupuncture on Mechanisms of Coronary Heart Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00570024

Link

https://clinicaltrials.gov/show/NCT00570024

Keywords

Versions (1)
  1. 2/25/17 2/25/17 -
Uploaded on

February 25, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00570024

English

Eligibility Coronary Artery Disease NCT00570024

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 21 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
local residence
Description

Local residence

Data type

boolean

Alias
UMLS CUI [1]
C0237096
medically able to participate
Description

Organ function

Data type

boolean

Alias
UMLS CUI [1]
C0678852
cad by mi, cabg, ptca, or stroke (>3 months prior), or angiographic evidence >50% epicardial coronary artery stenosis in at least one coronary artery
Description

Coronary artery disease or angiographic evidence

Data type

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2]
C0002971
consent and referring md approval
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
comorbid disease precluding survival during study
Description

Comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
mi, unstable angina, cabg, ptca or stroke within 3 months*
Description

MI, unstable angina, cabg, ptca or stroke

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0010055
UMLS CUI [4]
C2936173
UMLS CUI [5]
C0038454
hiv infection, chronic or active hepatitis or other blood-borne illness
Description

HIV infection, hepatitis, blood-borne illness

Data type

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0019158
UMLS CUI [3]
C1636665
cognitive, psychological or substance abuse-related impairment, as clinically assessed
Description

Cognitive, psychological or substance abuse-related impairment

Data type

boolean

Alias
UMLS CUI [1]
C1839000
UMLS CUI [2]
C0004936
UMLS CUI [3]
C0038586
atrial fibrillation, predominant pacemaker rhythm, significant conduction system disease, or automatic internal defibrillator*
Description

Arrhythmia

Data type

boolean

Alias
UMLS CUI [1]
C0003811
significant valvular heart disease*
Description

Valvular heart disease

Data type

boolean

Alias
UMLS CUI [1]
C0018824
class iii or iv heart failure*
Description

Heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018801
renal or liver failure, as clinically assessed
Description

Renal or liver failure

Data type

boolean

Alias
UMLS CUI [1]
C1533077
UMLS CUI [2]
C0085605
participating in ta, or formal psychosocial stress management program
Description

Mental health

Data type

boolean

Alias
UMLS CUI [1]
C0025353
participation in another trial.
Description

Study participation status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Coronary Artery Disease NCT00570024

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age > 21 years
boolean
C0001779 (UMLS CUI [1])
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Local residence
Item
local residence
boolean
C0237096 (UMLS CUI [1])
Organ function
Item
medically able to participate
boolean
C0678852 (UMLS CUI [1])
Coronary artery disease or angiographic evidence
Item
cad by mi, cabg, ptca, or stroke (>3 months prior), or angiographic evidence >50% epicardial coronary artery stenosis in at least one coronary artery
boolean
C1956346 (UMLS CUI [1])
C0002971 (UMLS CUI [2])
Informed consent
Item
consent and referring md approval
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Comorbidity
Item
comorbid disease precluding survival during study
boolean
C0009488 (UMLS CUI [1])
MI, unstable angina, cabg, ptca or stroke
Item
mi, unstable angina, cabg, ptca or stroke within 3 months*
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C2936173 (UMLS CUI [4])
C0038454 (UMLS CUI [5])
HIV infection, hepatitis, blood-borne illness
Item
hiv infection, chronic or active hepatitis or other blood-borne illness
boolean
C0019693 (UMLS CUI [1])
C0019158 (UMLS CUI [2])
C1636665 (UMLS CUI [3])
Cognitive, psychological or substance abuse-related impairment
Item
cognitive, psychological or substance abuse-related impairment, as clinically assessed
boolean
C1839000 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0038586 (UMLS CUI [3])
Arrhythmia
Item
atrial fibrillation, predominant pacemaker rhythm, significant conduction system disease, or automatic internal defibrillator*
boolean
C0003811 (UMLS CUI [1])
Valvular heart disease
Item
significant valvular heart disease*
boolean
C0018824 (UMLS CUI [1])
Heart failure
Item
class iii or iv heart failure*
boolean
C0018801 (UMLS CUI [1])
Renal or liver failure
Item
renal or liver failure, as clinically assessed
boolean
C1533077 (UMLS CUI [1])
C0085605 (UMLS CUI [2])
Mental health
Item
participating in ta, or formal psychosocial stress management program
boolean
C0025353 (UMLS CUI [1])
Study participation status
Item
participation in another trial.
boolean
C2348568 (UMLS CUI [1])
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