ID

34308

Beschrijving

Evaluation of CLP With and Without Spironolactone in Heart Failure Patients With Chronic Kidney Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01598740

Link

https://clinicaltrials.gov/show/NCT01598740

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Heart Failure NCT01598740

Eligibility Heart Failure NCT01598740

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
heart failure with new york heart association (nyha) classification ii or iii
Beschrijving

ID.1

Datatype

boolean

chronic kidney disease
Beschrijving

ID.2

Datatype

boolean

cardiac ejection fraction <40%
Beschrijving

ID.3

Datatype

boolean

on heart failure therapy including an acei or arb, and a bb
Beschrijving

ID.4

Datatype

boolean

willing to understand and comply with study procedures and provide written informed consent.
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
hospitalization within 4 weeks of baseline visit
Beschrijving

ID.6

Datatype

boolean

history or presence of gastrointestinal conditions such as severe constipation or gastrointestinal tract strictures
Beschrijving

ID.7

Datatype

boolean

current or anticipated dialysis during study
Beschrijving

ID.8

Datatype

boolean

in the investigator's judgment, any cardiovascular, renal, hepatic, endocrine, gastrointestinal, neurological, or other disease or condition that makes the subject's study participation unsafe
Beschrijving

ID.9

Datatype

boolean

drug or alcohol abuse
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Heart Failure NCT01598740

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
heart failure with new york heart association (nyha) classification ii or iii
boolean
ID.2
Item
chronic kidney disease
boolean
ID.3
Item
cardiac ejection fraction <40%
boolean
ID.4
Item
on heart failure therapy including an acei or arb, and a bb
boolean
ID.5
Item
willing to understand and comply with study procedures and provide written informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
hospitalization within 4 weeks of baseline visit
boolean
ID.7
Item
history or presence of gastrointestinal conditions such as severe constipation or gastrointestinal tract strictures
boolean
ID.8
Item
current or anticipated dialysis during study
boolean
ID.9
Item
in the investigator's judgment, any cardiovascular, renal, hepatic, endocrine, gastrointestinal, neurological, or other disease or condition that makes the subject's study participation unsafe
boolean
ID.10
Item
drug or alcohol abuse
boolean

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