ID

39387

Beschrijving

Comparing the Effects of Conivaptan and Diuretics on Plasma Neurohormones and Renal Blood Flow in Patients With Chronic Congestive Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00924014

Link

https://clinicaltrials.gov/show/NCT00924014

Trefwoorden

Versies (1)
  1. 06-01-20 06-01-20 -
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See clinicaltrials.gov

Geüploaded op

6 januari 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure NCT00924014

Engels

Eligibility Heart Failure NCT00924014

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
have a diagnosis of chronic congestive heart failure of any etiology
Beschrijving

Chronic congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0264722
be between 18-80 years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
able to provide consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
have a documented left ventricular ejection fraction within the last year of < 40%
Beschrijving

Left ventricular ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0428772
on a stable dose (no changes within 2 weeks) of 40 mg or greater daily dose of furosemide or its equivalent
Beschrijving

Furosemide Dose Stable U/day | Equivalent Dose Stable U/day

Datatype

boolean

Alias
UMLS CUI [1,1]
C0016860
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
UMLS CUI [1,4]
C0456683
UMLS CUI [2,1]
C0205163
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0205360
UMLS CUI [2,4]
C0456683
on standard hf therapy medications (acei or arb and beta-blocker unless contraindicated)
Beschrijving

Standard of Care Pharmaceutical Preparations Heart failure | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist | Adrenergic beta-Antagonists | Exception Medical contraindication

Datatype

boolean

Alias
UMLS CUI [1,1]
C2936643
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0018801
UMLS CUI [2]
C0003015
UMLS CUI [3]
C0521942
UMLS CUI [4]
C0001645
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C1301624
have an estimated glomerular filtration rate (gfr) of 30 ml/minute or greater (based on the cockcroft gault calculation)
Beschrijving

Estimated Glomerular Filtration Rate Cockcroft-Gault formula

Datatype

boolean

Alias
UMLS CUI [1,1]
C3811844
UMLS CUI [1,2]
C2924627
have a hemoglobin of > 10 grams/dl
Beschrijving

Hemoglobin measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0518015
have a negative urine pregnancy for women of childbearing years only
Beschrijving

Childbearing Potential Urine pregnancy test negative

Datatype

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0430057
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute coronary syndrome within 1 month
Beschrijving

Acute Coronary Syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0948089
systolic blood pressure less than or equal to 90 mmhg at time of enrollment
Beschrijving

Systolic Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
poor peripheral venous access
Beschrijving

Peripheral venous access Poor

Datatype

boolean

Alias
UMLS CUI [1,1]
C4489703
UMLS CUI [1,2]
C0542537
severe concomitant disease which deemed by the investigator would render them unsuitable for this trial
Beschrijving

Comorbidity Severe | Study Subject Participation Status Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C1548788
allergy or contraindication to the use of iothalamate, pah - specifically any allergies to iodine or iodine containing products, history of asthma and hay fever which deemed by the investigator would render them unsuitable for this trial
Beschrijving

Hypersensitivity Iothalamate | Medical contraindication Iothalamate | Hypersensitivity p-Aminohippuric Acid | Medical contraindication p-Aminohippuric Acid | Iodine allergy | Hypersensitivity Preparations Containing Iodine | Asthma | Hay fever | Study Subject Participation Status Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0022032
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0022032
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0030123
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C0030123
UMLS CUI [5]
C0571818
UMLS CUI [6,1]
C0020517
UMLS CUI [6,2]
C0013227
UMLS CUI [6,3]
C0332256
UMLS CUI [6,4]
C0021968
UMLS CUI [7]
C0004096
UMLS CUI [8]
C0018621
UMLS CUI [9,1]
C2348568
UMLS CUI [9,2]
C1548788
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Similar models

Eligibility Heart Failure NCT00924014

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Chronic congestive heart failure
Item
have a diagnosis of chronic congestive heart failure of any etiology
boolean
C0264722 (UMLS CUI [1])
Age
Item
be between 18-80 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
able to provide consent
boolean
C0021430 (UMLS CUI [1])
Left ventricular ejection fraction
Item
have a documented left ventricular ejection fraction within the last year of < 40%
boolean
C0428772 (UMLS CUI [1])
Furosemide Dose Stable U/day | Equivalent Dose Stable U/day
Item
on a stable dose (no changes within 2 weeks) of 40 mg or greater daily dose of furosemide or its equivalent
boolean
C0016860 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0456683 (UMLS CUI [1,4])
C0205163 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0205360 (UMLS CUI [2,3])
C0456683 (UMLS CUI [2,4])
Standard of Care Pharmaceutical Preparations Heart failure | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist | Adrenergic beta-Antagonists | Exception Medical contraindication
Item
on standard hf therapy medications (acei or arb and beta-blocker unless contraindicated)
boolean
C2936643 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
C0521942 (UMLS CUI [3])
C0001645 (UMLS CUI [4])
C1705847 (UMLS CUI [5,1])
C1301624 (UMLS CUI [5,2])
Estimated Glomerular Filtration Rate Cockcroft-Gault formula
Item
have an estimated glomerular filtration rate (gfr) of 30 ml/minute or greater (based on the cockcroft gault calculation)
boolean
C3811844 (UMLS CUI [1,1])
C2924627 (UMLS CUI [1,2])
Hemoglobin measurement
Item
have a hemoglobin of > 10 grams/dl
boolean
C0518015 (UMLS CUI [1])
Childbearing Potential Urine pregnancy test negative
Item
have a negative urine pregnancy for women of childbearing years only
boolean
C3831118 (UMLS CUI [1,1])
C0430057 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Acute Coronary Syndrome
Item
acute coronary syndrome within 1 month
boolean
C0948089 (UMLS CUI [1])
Systolic Pressure
Item
systolic blood pressure less than or equal to 90 mmhg at time of enrollment
boolean
C0871470 (UMLS CUI [1])
Peripheral venous access Poor
Item
poor peripheral venous access
boolean
C4489703 (UMLS CUI [1,1])
C0542537 (UMLS CUI [1,2])
Comorbidity Severe | Study Subject Participation Status Inappropriate
Item
severe concomitant disease which deemed by the investigator would render them unsuitable for this trial
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C1548788 (UMLS CUI [2,2])
Hypersensitivity Iothalamate | Medical contraindication Iothalamate | Hypersensitivity p-Aminohippuric Acid | Medical contraindication p-Aminohippuric Acid | Iodine allergy | Hypersensitivity Preparations Containing Iodine | Asthma | Hay fever | Study Subject Participation Status Inappropriate
Item
allergy or contraindication to the use of iothalamate, pah - specifically any allergies to iodine or iodine containing products, history of asthma and hay fever which deemed by the investigator would render them unsuitable for this trial
boolean
C0020517 (UMLS CUI [1,1])
C0022032 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0022032 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0030123 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C0030123 (UMLS CUI [4,2])
C0571818 (UMLS CUI [5])
C0020517 (UMLS CUI [6,1])
C0013227 (UMLS CUI [6,2])
C0332256 (UMLS CUI [6,3])
C0021968 (UMLS CUI [6,4])
C0004096 (UMLS CUI [7])
C0018621 (UMLS CUI [8])
C2348568 (UMLS CUI [9,1])
C1548788 (UMLS CUI [9,2])
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