ID

29889

Description

The Efficacy of Spironolactone in Patients With Resistant Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00430794

Lien

https://clinicaltrials.gov/show/NCT00430794

Mots-clés

Versions (1)
  1. 25/04/2018 25/04/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

25 avril 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Hypertension NCT00430794

Anglais

Eligibility Hypertension NCT00430794

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged over 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
hypertension (essential or secondary) managed in sheffield hypertension clinic or general practice or both.
Description

Essential Hypertension | Secondary hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C0085580
UMLS CUI [2]
C0155616
blood pressures not adequately controlled (systolic blood pressure (sbp) >140 mmhg and/or diastolic blood pressure (dbp) >85 mmhg in clinic and on ambulatory blood pressure monitoring) despite treatment with the maximum tolerated dose of three antihypertensive agents.
Description

Blood Pressure Poorly controlled | Systolic Pressure | Diastolic blood pressure | Antihypertensive Agents Quantity Maximum Tolerated Dose

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C3853134
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C1265611
UMLS CUI [4,3]
C0752079
additional antihypertensive treatment deemed appropriate by the patients' doctor.
Description

Antihypertensive therapy Additional Appropriate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C1524062
UMLS CUI [1,3]
C1548787
patients' current antihypertensive treatment includes a thiazide diuretic and at least one of a beta-blocker, angiotensin converting enzyme inhibitor or angiotensin ii receptor antagonist.
Description

Antihypertensive therapy | Thiazide Diuretic | Adrenergic beta-1 Receptor Antagonists Quantity | Angiotensin-Converting Enzyme Inhibitors Quantity | Angiotensin II receptor antagonist Quantity

Type de données

boolean

Alias
UMLS CUI [1]
C0585941
UMLS CUI [2]
C0012802
UMLS CUI [3,1]
C0304516
UMLS CUI [3,2]
C1265611
UMLS CUI [4,1]
C0003015
UMLS CUI [4,2]
C1265611
UMLS CUI [5,1]
C0521942
UMLS CUI [5,2]
C1265611
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
definite indication or contraindication for spironolactone
Description

Indication Spironolactone | Medical contraindication Spironolactone

Type de données

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0037982
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0037982
known conn's syndrome (definite indication for spironolactone)
Description

Conn Syndrome | Indication Spironolactone

Type de données

boolean

Alias
UMLS CUI [1]
C1384514
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0037982
heart failure nyha class iii or iv (definite indication for spironolactone)
Description

Heart failure New York Heart Association Classification | Indication Spironolactone

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0037982
known hepatic failure or significant cirrhosis
Description

Liver Failure | Liver Cirrhosis

Type de données

boolean

Alias
UMLS CUI [1]
C0085605
UMLS CUI [2]
C0023890
known pregnancy or women planning pregnancy
Description

Pregnancy | Pregnancy, Planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
women of child bearing potential not using adequate contraceptive methods
Description

Childbearing Potential Contraceptive methods Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332197
serum creatinine > 221µmol/l
Description

Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
serum potassium > 5.0mmol/l
Description

Serum potassium measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0302353
clinic blood pressure or daytime ambulatory blood pressure >240/120
Description

Blood pressure determination Clinic | Blood pressure ambulatory Daytime

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005824
UMLS CUI [1,2]
C0442592
UMLS CUI [2,1]
C0855316
UMLS CUI [2,2]
C0332169
Retour au début de la page

Similar models

Eligibility Hypertension NCT00430794

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged over 18 years
boolean
C0001779 (UMLS CUI [1])
Essential Hypertension | Secondary hypertension
Item
hypertension (essential or secondary) managed in sheffield hypertension clinic or general practice or both.
boolean
C0085580 (UMLS CUI [1])
C0155616 (UMLS CUI [2])
Blood Pressure Poorly controlled | Systolic Pressure | Diastolic blood pressure | Antihypertensive Agents Quantity Maximum Tolerated Dose
Item
blood pressures not adequately controlled (systolic blood pressure (sbp) >140 mmhg and/or diastolic blood pressure (dbp) >85 mmhg in clinic and on ambulatory blood pressure monitoring) despite treatment with the maximum tolerated dose of three antihypertensive agents.
boolean
C0005823 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0003364 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0752079 (UMLS CUI [4,3])
Antihypertensive therapy Additional Appropriate
Item
additional antihypertensive treatment deemed appropriate by the patients' doctor.
boolean
C0585941 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C1548787 (UMLS CUI [1,3])
Antihypertensive therapy | Thiazide Diuretic | Adrenergic beta-1 Receptor Antagonists Quantity | Angiotensin-Converting Enzyme Inhibitors Quantity | Angiotensin II receptor antagonist Quantity
Item
patients' current antihypertensive treatment includes a thiazide diuretic and at least one of a beta-blocker, angiotensin converting enzyme inhibitor or angiotensin ii receptor antagonist.
boolean
C0585941 (UMLS CUI [1])
C0012802 (UMLS CUI [2])
C0304516 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0003015 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0521942 (UMLS CUI [5,1])
C1265611 (UMLS CUI [5,2])
Item Group
C0680251 (UMLS CUI)
Indication Spironolactone | Medical contraindication Spironolactone
Item
definite indication or contraindication for spironolactone
boolean
C3146298 (UMLS CUI [1,1])
C0037982 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0037982 (UMLS CUI [2,2])
Conn Syndrome | Indication Spironolactone
Item
known conn's syndrome (definite indication for spironolactone)
boolean
C1384514 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C0037982 (UMLS CUI [2,2])
Heart failure New York Heart Association Classification | Indication Spironolactone
Item
heart failure nyha class iii or iv (definite indication for spironolactone)
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0037982 (UMLS CUI [2,2])
Liver Failure | Liver Cirrhosis
Item
known hepatic failure or significant cirrhosis
boolean
C0085605 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
Pregnancy | Pregnancy, Planned
Item
known pregnancy or women planning pregnancy
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Absent
Item
women of child bearing potential not using adequate contraceptive methods
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Creatinine measurement, serum
Item
serum creatinine > 221µmol/l
boolean
C0201976 (UMLS CUI [1])
Serum potassium measurement
Item
serum potassium > 5.0mmol/l
boolean
C0302353 (UMLS CUI [1])
Blood pressure determination Clinic | Blood pressure ambulatory Daytime
Item
clinic blood pressure or daytime ambulatory blood pressure >240/120
boolean
C0005824 (UMLS CUI [1,1])
C0442592 (UMLS CUI [1,2])
C0855316 (UMLS CUI [2,1])
C0332169 (UMLS CUI [2,2])
Retour au début de la page 

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