ID

40031

Beschrijving

Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01438229

Link

https://clinicaltrials.gov/show/NCT01438229

Trefwoorden

Versies (1)
  1. 10-03-20 10-03-20 -
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See clinicaltrials.gov

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10 maart 2020

DOI

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Creative Commons BY 4.0
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Eligibility Hypertension NCT01438229

Engels

Eligibility Hypertension NCT01438229

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
office systolic blood pressure that remains ≥160 mmhg (≥150 mmhg for patient with type 2 diabetes) despite the stable use of ≥3 antihypertensive medications concurrently at maximally tolerated doses, of which one is a diuretic, for a minimum of 14 days prior to enrollment
Beschrijving

Systolic Pressure | Diabetes Mellitus, Non-Insulin-Dependent | Antihypertensive Agents Quantity | Antihypertensive Agents Maximum Tolerated Dose Stable | Diuretics

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0011860
UMLS CUI [3,1]
C0003364
UMLS CUI [3,2]
C1265611
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C0752079
UMLS CUI [4,3]
C0205360
UMLS CUI [5]
C0012798
age ≥18 and ≤80 years old
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
able and willing to provide written informed consent to participate in the study
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
able and willing to comply with the required follow-up schedule
Beschrijving

Compliance Follow-up

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C3274571
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior renal artery intervention (balloon angioplasty or stenting)
Beschrijving

Renal artery Intervention | Angioplasty, Balloon | Stenting

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C0184661
UMLS CUI [2]
C0002996
UMLS CUI [3]
C2348535
evidence of renal artery atherosclerosis (defined as a stenotic severity of >30%) in either renal artery
Beschrijving

Atherosclerosis of renal artery

Datatype

boolean

Alias
UMLS CUI [1]
C0155734
multiple main renal arteries in either kidney
Beschrijving

Renal artery Main Multiple | Kidney Either

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C1542147
UMLS CUI [1,3]
C0439064
UMLS CUI [2,1]
C0022646
UMLS CUI [2,2]
C3844638
main renal arteries <4 mm in diameter or <20 mm in length
Beschrijving

Renal artery Main Diameter | Renal artery Main Length

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C1542147
UMLS CUI [1,3]
C1301886
UMLS CUI [2,1]
C0035065
UMLS CUI [2,2]
C1542147
UMLS CUI [2,3]
C1444754
egfr of <45 ml/min per 1.73 m2 using the mdrd formula
Beschrijving

GFR estimation by MDRD

Datatype

boolean

Alias
UMLS CUI [1]
C2170215
type 1 diabetes
Beschrijving

Diabetes Mellitus, Insulin-Dependent

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
renovascular hypertension or hypertension secondary to other renal disorders (glomerulonephritis, polycystic kidney disease, end-stage renal failure)
Beschrijving

Hypertension, Renovascular | Hypertensive disease Secondary to Kidney Diseases | Glomerulonephritis | Polycystic Kidney Diseases | Kidney Failure, Chronic

Datatype

boolean

Alias
UMLS CUI [1]
C0020545
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C0175668
UMLS CUI [2,3]
C0022658
UMLS CUI [3]
C0017658
UMLS CUI [4]
C0022680
UMLS CUI [5]
C0022661
others
Beschrijving

Exclusion Criteria Additional

Datatype

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1524062
Terug naar het begin van de pagina

Similar models

Eligibility Hypertension NCT01438229

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Systolic Pressure | Diabetes Mellitus, Non-Insulin-Dependent | Antihypertensive Agents Quantity | Antihypertensive Agents Maximum Tolerated Dose Stable | Diuretics
Item
office systolic blood pressure that remains ≥160 mmhg (≥150 mmhg for patient with type 2 diabetes) despite the stable use of ≥3 antihypertensive medications concurrently at maximally tolerated doses, of which one is a diuretic, for a minimum of 14 days prior to enrollment
boolean
C0871470 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0003364 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0003364 (UMLS CUI [4,1])
C0752079 (UMLS CUI [4,2])
C0205360 (UMLS CUI [4,3])
C0012798 (UMLS CUI [5])
Age
Item
age ≥18 and ≤80 years old
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
able and willing to provide written informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
Compliance Follow-up
Item
able and willing to comply with the required follow-up schedule
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Renal artery Intervention | Angioplasty, Balloon | Stenting
Item
prior renal artery intervention (balloon angioplasty or stenting)
boolean
C0035065 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C0002996 (UMLS CUI [2])
C2348535 (UMLS CUI [3])
Atherosclerosis of renal artery
Item
evidence of renal artery atherosclerosis (defined as a stenotic severity of >30%) in either renal artery
boolean
C0155734 (UMLS CUI [1])
Renal artery Main Multiple | Kidney Either
Item
multiple main renal arteries in either kidney
boolean
C0035065 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
C0439064 (UMLS CUI [1,3])
C0022646 (UMLS CUI [2,1])
C3844638 (UMLS CUI [2,2])
Renal artery Main Diameter | Renal artery Main Length
Item
main renal arteries <4 mm in diameter or <20 mm in length
boolean
C0035065 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0035065 (UMLS CUI [2,1])
C1542147 (UMLS CUI [2,2])
C1444754 (UMLS CUI [2,3])
GFR estimation by MDRD
Item
egfr of <45 ml/min per 1.73 m2 using the mdrd formula
boolean
C2170215 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Hypertension, Renovascular | Hypertensive disease Secondary to Kidney Diseases | Glomerulonephritis | Polycystic Kidney Diseases | Kidney Failure, Chronic
Item
renovascular hypertension or hypertension secondary to other renal disorders (glomerulonephritis, polycystic kidney disease, end-stage renal failure)
boolean
C0020545 (UMLS CUI [1])
C0020538 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0022658 (UMLS CUI [2,3])
C0017658 (UMLS CUI [3])
C0022680 (UMLS CUI [4])
C0022661 (UMLS CUI [5])
Exclusion Criteria Additional
Item
others
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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