Eligibility End Stage Renal Disease NCT00551304

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult >= 18 years of age
Description

Adult | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
end stage renal disease, undergoing concurrent dialysis treatment
Description

Kidney Failure, Chronic | Dialysis

Type de données

boolean

Alias
UMLS CUI [1]
C0022661
UMLS CUI [2]
C0011946
poorly controlled blood pressure on at least 2 antihypertensive drugs
Description

Blood Pressure Poorly controlled | Antihypertensive Agents Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C3853134
UMLS CUI [2,1]
C0003364
UMLS CUI [2,2]
C1265611
agrees to have the study procedure(s) performed and additional procedures and evaluations, including interventions and follow up visits
Description

Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1]
C0525058
competent and willing to provide written, informed consent to participate in this clinical study.
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
renal arterial abnormalities
Description

Abnormality of the renal artery

Type de données

boolean

Alias
UMLS CUI [1]
C4024624
myocardial infarction, unstable angina pectoris, or a cerebrovascular accident within six (6) months
Description

Myocardial Infarction | Angina, Unstable | Cerebrovascular accident

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
hemodynamically significant valvular heart disease
Description

Heart valve disease Hemodynamics Significant

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0019010
UMLS CUI [1,3]
C0750502
implantable cardioverter defibrillator (icd) or pacemaker
Description

Implantable defibrillator | Artificial cardiac pacemaker

Type de données

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0030163
respiratory support.
Description

Support respiratory

Type de données

boolean

Alias
UMLS CUI [1,1]
C1521721
UMLS CUI [1,2]
C0521346
pregnant, nursing or planning to be pregnant
Description

Pregnancy | Breast Feeding | Pregnancy, Planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
other
Description

Exclusion Criteria Additional

Type de données

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1524062

Similar models

Eligibility End Stage Renal Disease NCT00551304

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult >= 18 years of age
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Kidney Failure, Chronic | Dialysis
Item
end stage renal disease, undergoing concurrent dialysis treatment
boolean
C0022661 (UMLS CUI [1])
C0011946 (UMLS CUI [2])
Blood Pressure Poorly controlled | Antihypertensive Agents Quantity
Item
poorly controlled blood pressure on at least 2 antihypertensive drugs
boolean
C0005823 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0003364 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
Protocol Compliance
Item
agrees to have the study procedure(s) performed and additional procedures and evaluations, including interventions and follow up visits
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
competent and willing to provide written, informed consent to participate in this clinical study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Abnormality of the renal artery
Item
renal arterial abnormalities
boolean
C4024624 (UMLS CUI [1])
Myocardial Infarction | Angina, Unstable | Cerebrovascular accident
Item
myocardial infarction, unstable angina pectoris, or a cerebrovascular accident within six (6) months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Heart valve disease Hemodynamics Significant
Item
hemodynamically significant valvular heart disease
boolean
C0018824 (UMLS CUI [1,1])
C0019010 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,3])
Implantable defibrillator | Artificial cardiac pacemaker
Item
implantable cardioverter defibrillator (icd) or pacemaker
boolean
C0162589 (UMLS CUI [1])
C0030163 (UMLS CUI [2])
Support respiratory
Item
respiratory support.
boolean
C1521721 (UMLS CUI [1,1])
C0521346 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
pregnant, nursing or planning to be pregnant
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Exclusion Criteria Additional
Item
other
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])