ID

29935

Descripción

Renal Denervation in Patients With Refractory Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00664638

Link

https://clinicaltrials.gov/show/NCT00664638

Palabras clave

Versiones (1)
  1. 27/4/18 27/4/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

27 de abril de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Hypertension NCT00664638

Inglés

Eligibility Hypertension NCT00664638

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
>= 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
a systolic blood pressure of 160mmhg or more
Descripción

Systolic Pressure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0871470
receiving and adhering to full doses of at least three antihypertensive drugs
Descripción

Antihypertensive Agents Quantity Dose Full

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C0443225
estimated glomerular filtration rate (egfr) of ≥45ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

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

Protocol Compliance

Tipo de datos

boolean

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

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
hemodynamically or anatomically significant renal artery stenosis
Descripción

Renal Artery Stenosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0035067
has a history or prior renal artery angioplasty
Descripción

Angioplasty renal artery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1282893
has experienced mi, unstable angina pectoris, or cva within 6 months
Descripción

Myocardial Infarction | Angina, Unstable | Cerebrovascular accident

Tipo de datos

boolean

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

Heart valve disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018824
has type 1 diabetes
Descripción

Diabetes Mellitus, Insulin-Dependent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011854
has an implantable cardioverter defibrillator (icd) or pacemaker, or any other metallic implant which is not compatible with magnetic resonance imaging (mri)
Descripción

Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Incompatibility Problem MRI

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0030163
UMLS CUI [3,1]
C3693688
UMLS CUI [3,2]
C1881693
UMLS CUI [3,3]
C0024485
requires respiratory support
Descripción

Patient need for Support respiratory

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C0344211
UMLS CUI [1,3]
C0521346
is pregnant, nursing, or planning to be pregnant
Descripción

Pregnancy | Breast Feeding | Pregnancy, Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
has known, unresolved history of drug use or alcohol dependency.
Descripción

Drug usage | Alcoholic Intoxication, Chronic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0242510
UMLS CUI [2]
C0001973
is currently enrolled in another investigational drug or device trial.
Descripción

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
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Similar models

Eligibility Hypertension NCT00664638

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
>= 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
a systolic blood pressure of 160mmhg or more
boolean
C0871470 (UMLS CUI [1])
Antihypertensive Agents Quantity Dose Full
Item
receiving and adhering to full doses of at least three antihypertensive drugs
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0443225 (UMLS CUI [1,4])
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)
Renal Artery Stenosis
Item
hemodynamically or anatomically significant renal artery stenosis
boolean
C0035067 (UMLS CUI [1])
Angioplasty renal artery
Item
has a history or prior renal artery angioplasty
boolean
C1282893 (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])
Heart valve disease
Item
has hemodynamically significant valvular heart disease
boolean
C0018824 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
has type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Incompatibility Problem MRI
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])
C1881693 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
Patient need for Support respiratory
Item
requires respiratory support
boolean
C0686904 (UMLS CUI [1,1])
C0344211 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
is pregnant, nursing, or planning to be pregnant
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Drug usage | Alcoholic Intoxication, Chronic
Item
has known, unresolved history of drug use or alcohol dependency.
boolean
C0242510 (UMLS CUI [1])
C0001973 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
is currently enrolled in another investigational drug or device trial.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
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