ID

34307

Beschrijving

Study to Evaluate TRV120027 on Renal Pharmacodynamics in Patients With Heart Failure and Renal Dysfunction; ODM derived from: https://clinicaltrials.gov/show/NCT01444872

Link

https://clinicaltrials.gov/show/NCT01444872

Trefwoorden

  1. 16-01-19 16-01-19 -
  2. 05-10-20 05-10-20 -
  3. 07-10-20 07-10-20 -
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 NCT01444872

Eligibility Heart Failure NCT01444872

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
written informed consent
Beschrijving

ID.1

Datatype

boolean

heart failure
Beschrijving

ID.2

Datatype

boolean

mild to moderate renal dysfunction
Beschrijving

ID.3

Datatype

boolean

age 18- <75
Beschrijving

ID.4

Datatype

boolean

males and females (non-childbearing potential)
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
any significant disease or condition that would interfere with the interpretation of safety or efficacy or efficacy data as determined by the investigator based on medical history, physical examination or laboratory tests
Beschrijving

ID.6

Datatype

boolean

any other serious life threatening disease that may impair the interpretation of safety or efficacy data from the study as determined by the investigator
Beschrijving

ID.7

Datatype

boolean

allergy or clinically-significant intolerance to arbs or ace inhibitors
Beschrijving

ID.8

Datatype

boolean

clinical signs or symptoms of acute decompensated heart failure
Beschrijving

ID.9

Datatype

boolean

pregnant or lactating
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Heart Failure NCT01444872

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
written informed consent
boolean
ID.2
Item
heart failure
boolean
ID.3
Item
mild to moderate renal dysfunction
boolean
ID.4
Item
age 18- <75
boolean
ID.5
Item
males and females (non-childbearing potential)
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
any significant disease or condition that would interfere with the interpretation of safety or efficacy or efficacy data as determined by the investigator based on medical history, physical examination or laboratory tests
boolean
ID.7
Item
any other serious life threatening disease that may impair the interpretation of safety or efficacy data from the study as determined by the investigator
boolean
ID.8
Item
allergy or clinically-significant intolerance to arbs or ace inhibitors
boolean
ID.9
Item
clinical signs or symptoms of acute decompensated heart failure
boolean
ID.10
Item
pregnant or lactating
boolean

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