ID

29942

Description

Spironolactone Versus Amiloride as an Add on Agent in Resistant Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00709137

Link

https://clinicaltrials.gov/show/NCT00709137

Keywords

Versions (1)
  1. 4/28/18 4/28/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

April 28, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Hypertension NCT00709137

English

Eligibility Hypertension NCT00709137

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
participants will be selected from a broad range of medical clinics at the salt lake city va medical center and surrounding community based outpatient clinics (cbocs).
Description

Patient Recruitment Clinics

Data type

boolean

Alias
UMLS CUI [1,1]
C0242800
UMLS CUI [1,2]
C0442592
the participants will be referred to a resistant hypertension clinic by either their primary care provider or by a subspecialist. the referrals are made via a computerized system that is used in the veterans affairs medical center (va) called computerized patient record system (cprs).
Description

Study Subject Referral to RESISTANT HYPERTENSION Clinic

Data type

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C2585021
UMLS CUI [1,3]
C0745130
UMLS CUI [1,4]
C0442592
patients are referred if their blood pressure is above goal as defined by jnc 7 and they are on 3 antihypertensive medications with one of the agents being a diuretic.
Description

Blood pressure determination | Antihypertensive Agents Quantity | Diuretics Quantity

Data type

boolean

Alias
UMLS CUI [1]
C0005824
UMLS CUI [2,1]
C0003364
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0012798
UMLS CUI [3,2]
C1265611
all patients age 18 -80 years old.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients that will be excluded from the study if they have had a documented adverse reaction to either spironolactone or amiloride.
Description

Spironolactone adverse reaction | Amiloride adverse reaction

Data type

boolean

Alias
UMLS CUI [1]
C0414009
UMLS CUI [2]
C0414008
diagnosis of primary hyperaldosteronism
Description

Conn Syndrome

Data type

boolean

Alias
UMLS CUI [1]
C1384514
inability to adhere to frequent laboratory monitoring
Description

Monitoring of laboratory results Frequent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C3165364
UMLS CUI [1,2]
C0332183
UMLS CUI [1,3]
C1299582
estimated glomerular filtration rate (gfr) < 45 ml/min/1.73m2
Description

Estimated Glomerular Filtration Rate

Data type

boolean

Alias
UMLS CUI [1]
C3811844
baseline serum potassium above 5.0 meq/l
Description

Serum potassium measurement

Data type

boolean

Alias
UMLS CUI [1]
C0302353
type 4 renal tubular acidosis
Description

Renal tubular acidosis Type

Data type

boolean

Alias
UMLS CUI [1,1]
C0001126
UMLS CUI [1,2]
C0332307
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
heart failure that meets criteria for using either eplerenone or spironolactone
Description

Heart failure | Eplerenone | Spironolactone

Data type

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C0961485
UMLS CUI [3]
C0037982
current unstable renal function
Description

Renal function Unstable

Data type

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0443343
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Similar models

Eligibility Hypertension NCT00709137

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Patient Recruitment Clinics
Item
participants will be selected from a broad range of medical clinics at the salt lake city va medical center and surrounding community based outpatient clinics (cbocs).
boolean
C0242800 (UMLS CUI [1,1])
C0442592 (UMLS CUI [1,2])
Study Subject Referral to RESISTANT HYPERTENSION Clinic
Item
the participants will be referred to a resistant hypertension clinic by either their primary care provider or by a subspecialist. the referrals are made via a computerized system that is used in the veterans affairs medical center (va) called computerized patient record system (cprs).
boolean
C0681850 (UMLS CUI [1,1])
C2585021 (UMLS CUI [1,2])
C0745130 (UMLS CUI [1,3])
C0442592 (UMLS CUI [1,4])
Blood pressure determination | Antihypertensive Agents Quantity | Diuretics Quantity
Item
patients are referred if their blood pressure is above goal as defined by jnc 7 and they are on 3 antihypertensive medications with one of the agents being a diuretic.
boolean
C0005824 (UMLS CUI [1])
C0003364 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0012798 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Age
Item
all patients age 18 -80 years old.
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Spironolactone adverse reaction | Amiloride adverse reaction
Item
patients that will be excluded from the study if they have had a documented adverse reaction to either spironolactone or amiloride.
boolean
C0414009 (UMLS CUI [1])
C0414008 (UMLS CUI [2])
Conn Syndrome
Item
diagnosis of primary hyperaldosteronism
boolean
C1384514 (UMLS CUI [1])
Monitoring of laboratory results Frequent Unable
Item
inability to adhere to frequent laboratory monitoring
boolean
C3165364 (UMLS CUI [1,1])
C0332183 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (gfr) < 45 ml/min/1.73m2
boolean
C3811844 (UMLS CUI [1])
Serum potassium measurement
Item
baseline serum potassium above 5.0 meq/l
boolean
C0302353 (UMLS CUI [1])
Renal tubular acidosis Type
Item
type 4 renal tubular acidosis
boolean
C0001126 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Heart failure | Eplerenone | Spironolactone
Item
heart failure that meets criteria for using either eplerenone or spironolactone
boolean
C0018801 (UMLS CUI [1])
C0961485 (UMLS CUI [2])
C0037982 (UMLS CUI [3])
Renal function Unstable
Item
current unstable renal function
boolean
C0232804 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
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