ID

39996

Description

Renal Denervation in Patients With Uncontrolled Hypertension in Chinese; ODM derived from: https://clinicaltrials.gov/show/NCT01390831

Link

https://clinicaltrials.gov/show/NCT01390831

Keywords

  1. 3/8/20 3/8/20 -
  2. 3/9/20 3/9/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 9, 2020

DOI

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License

Creative Commons BY 4.0

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Eligibility Hypertension NCT01390831

Eligibility Hypertension NCT01390831

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
>= 18 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
a systolic blood pressure of 160mmhg or more and/or a diastolic blood pressure of 90mmhg or more
Description

Systolic Pressure | Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
receiving and adhering to at least three full doses of appropriate antihypertensive drug regimen
Description

Antihypertensive therapy Dose Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1265611
estimated glomerular filtration rate (egfr) of ≥45ml/min
Description

Estimated Glomerular Filtration Rate

Data type

boolean

Alias
UMLS CUI [1]
C3811844
agrees to have the study procedure(s) performed and additional procedures and evaluations
Description

Protocol Compliance

Data type

boolean

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

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary hypertension
Description

Secondary hypertension

Data type

boolean

Alias
UMLS CUI [1]
C0155616
renal arterial abnormalities
Description

Abnormal renal artery morphology

Data type

boolean

Alias
UMLS CUI [1]
C4024624
has experienced mi, unstable angina pectoris, or cva within 6 months
Description

Myocardial Infarction | Angina, Unstable | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
has an implantable cardioverter defibrillator (icd) or pacemaker, or any other metallic implant which is not compatible with magnetic resonance imaging (mri)
Description

Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Inconsistent Magnetic Resonance Imaging

Data type

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0030163
UMLS CUI [3,1]
C3693688
UMLS CUI [3,2]
C0442809
UMLS CUI [3,3]
C0024485
requires respiratory support
Description

Requirement Support respiratory

Data type

boolean

Alias
UMLS CUI [1,1]
C1514873
UMLS CUI [1,2]
C1521721
UMLS CUI [1,3]
C0521346
patients with sick sinus syndrome
Description

Sick Sinus Syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0037052
pregnant woman
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
others
Description

Exclusion Criteria Additional

Data type

boolean

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

Similar models

Eligibility Hypertension NCT01390831

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
>= 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure
Item
a systolic blood pressure of 160mmhg or more and/or a diastolic blood pressure of 90mmhg or more
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Antihypertensive therapy Dose Quantity
Item
receiving and adhering to at least three full doses of appropriate antihypertensive drug regimen
boolean
C0585941 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of ≥45ml/min
boolean
C3811844 (UMLS CUI [1])
Protocol Compliance
Item
agrees to have the study procedure(s) performed and additional procedures and evaluations
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
is competent and willing to provide written, informed consent to participate in this clinical study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Abnormal renal artery morphology
Item
renal arterial abnormalities
boolean
C4024624 (UMLS CUI [1])
Myocardial Infarction | Angina, Unstable | Cerebrovascular accident
Item
has experienced mi, unstable angina pectoris, or cva within 6 months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Inconsistent Magnetic Resonance Imaging
Item
has an implantable cardioverter defibrillator (icd) or pacemaker, or any other metallic implant which is not compatible with magnetic resonance imaging (mri)
boolean
C0162589 (UMLS CUI [1])
C0030163 (UMLS CUI [2])
C3693688 (UMLS CUI [3,1])
C0442809 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
Requirement Support respiratory
Item
requires respiratory support
boolean
C1514873 (UMLS CUI [1,1])
C1521721 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
Sick Sinus Syndrome
Item
patients with sick sinus syndrome
boolean
C0037052 (UMLS CUI [1])
Pregnancy
Item
pregnant woman
boolean
C0032961 (UMLS CUI [1])
Exclusion Criteria Additional
Item
others
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])

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