ID

39232

Descripción

Renal Sympathetic Modification in Patients With Essential Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01417221

Link

https://clinicaltrials.gov/show/NCT01417221

Palabras clave

Versiones (1)
  1. 11/12/19 11/12/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

11 de diciembre de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT01417221

Inglés

Eligibility Essential Hypertension NCT01417221

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
≥ 18 years old, and ≤ 75 years old of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
more than half a year history of hypertension, except for valvular heart disease
Descripción

Hypertensive disease Disease length | Exception Heart valve disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0872146
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018824
recently at least three times office blood pressure suggest systolic blood pressure of 140mmhg or more and/or a diastolic blood pressure of 90mmhg or more
Descripción

Office Blood pressure determination Times | Suggestion Systolic Pressure | Suggestion Diastolic blood pressure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0031834
UMLS CUI [1,2]
C0005824
UMLS CUI [1,3]
C1632851
UMLS CUI [2,1]
C1705535
UMLS CUI [2,2]
C0871470
UMLS CUI [3,1]
C1705535
UMLS CUI [3,2]
C0428883
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
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
secondary hypertension
Descripción

Secondary hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155616
estimated glomerular filtration rate (egfr) of < 45ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
has the history of renal restenosis or renal stents implantation
Descripción

Renal artery Restenosis | Insertion of renal artery stent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C0333186
UMLS CUI [2]
C1532969
has experienced ami (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
Descripción

Acute myocardial infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155626
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0017181
patients with sick sinus syndrome
Descripción

Sick Sinus Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0037052
pregnant women
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
mental disorders
Descripción

Mental disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
patients that have allergy to contrast agent
Descripción

Contrast media allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0570562
patients that do not go with follow-up
Descripción

Patients Follow-up failed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3274571
UMLS CUI [1,3]
C0231175
others such as researcher considers it is not appropriate to be included into the study
Descripción

Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
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Similar models

Eligibility Essential Hypertension NCT01417221

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
≥ 18 years old, and ≤ 75 years old of age
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease Disease length | Exception Heart valve disease
Item
more than half a year history of hypertension, except for valvular heart disease
boolean
C0020538 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0018824 (UMLS CUI [2,2])
Office Blood pressure determination Times | Suggestion Systolic Pressure | Suggestion Diastolic blood pressure
Item
recently at least three times office blood pressure suggest systolic blood pressure of 140mmhg or more and/or a diastolic blood pressure of 90mmhg or more
boolean
C0031834 (UMLS CUI [1,1])
C0005824 (UMLS CUI [1,2])
C1632851 (UMLS CUI [1,3])
C1705535 (UMLS CUI [2,1])
C0871470 (UMLS CUI [2,2])
C1705535 (UMLS CUI [3,1])
C0428883 (UMLS CUI [3,2])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
boolean
C3811844 (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])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of < 45ml/min
boolean
C3811844 (UMLS CUI [1])
Renal artery Restenosis | Insertion of renal artery stent
Item
has the history of renal restenosis or renal stents implantation
boolean
C0035065 (UMLS CUI [1,1])
C0333186 (UMLS CUI [1,2])
C1532969 (UMLS CUI [2])
Acute myocardial infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage
Item
has experienced ami (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
boolean
C0155626 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0017181 (UMLS CUI [4])
Sick Sinus Syndrome
Item
patients with sick sinus syndrome
boolean
C0037052 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Mental disorders
Item
mental disorders
boolean
C0004936 (UMLS CUI [1])
Contrast media allergy
Item
patients that have allergy to contrast agent
boolean
C0570562 (UMLS CUI [1])
Patients Follow-up failed
Item
patients that do not go with follow-up
boolean
C0030705 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Study Subject Participation Status Inappropriate
Item
others such as researcher considers it is not appropriate to be included into the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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