ID

12602

Beschrijving

Efficacy and Safety of Levosimendan in Severe Acute Heart Failure in Critical Children; ODM derived from: https://clinicaltrials.gov/show/NCT01301313

Link

https://clinicaltrials.gov/show/NCT01301313

Trefwoorden

  1. 04-12-15 04-12-15 -
Geüploaded op

4 december 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Heart Failure NCT01301313

Eligibility Acute Heart Failure NCT01301313

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who give written consent to participate in the study and for the transfer of material for cellular and molecular studies.
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
understand the purpose of the study and to be available to perform the procedures written in the protocol.
Beschrijving

understand the purpose of the study and to be available to perform the procedures written in the protocol

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
any child of 1 day old to 18 years old, admitted to the paediatric intensive care unit due to severe acute heart failure of any etiology.
Beschrijving

any child of 1 day old to 18 years old with acute heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0264714
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
Patients who express their wish of not to participate in the protocol
Beschrijving

Informed consent denied

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
hypertrophic or restrictive cardiomyopathy
Beschrijving

cardiomyopathy

Datatype

boolean

Alias
UMLS CUI [1]
C0878544
aortic stenosis
Beschrijving

aortic stenosis

Datatype

boolean

Alias
UMLS CUI [1]
C0003507
allergy to any drug used in the study
Beschrijving

allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0020517
it is not possible to prescribe the study medication because it is contraindicated according to the summary of the product characteristic or according to the criteria of the physician responsible for patient
Beschrijving

it is not possible to prescribe the study medication because it is contraindicated according to the summary of the product characteristic or according to the criteria of the physician responsible for patient

Datatype

boolean

Alias
UMLS CUI [1]
C1301624
UMLS CUI [2]
C0009488
Pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0549206

Similar models

Eligibility Acute Heart Failure NCT01301313

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Informed consent
Item
patients who give written consent to participate in the study and for the transfer of material for cellular and molecular studies.
boolean
C0021430 (UMLS CUI [1])
understand the purpose of the study and to be available to perform the procedures written in the protocol
Item
understand the purpose of the study and to be available to perform the procedures written in the protocol.
boolean
C1321605 (UMLS CUI [1])
any child of 1 day old to 18 years old with acute heart failure
Item
any child of 1 day old to 18 years old, admitted to the paediatric intensive care unit due to severe acute heart failure of any etiology.
boolean
C0001779 (UMLS CUI [1])
C0264714 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Informed consent denied
Item
Patients who express their wish of not to participate in the protocol
boolean
C0021430 (UMLS CUI [1])
cardiomyopathy
Item
hypertrophic or restrictive cardiomyopathy
boolean
C0878544 (UMLS CUI [1])
aortic stenosis
Item
aortic stenosis
boolean
C0003507 (UMLS CUI [1])
allergy
Item
allergy to any drug used in the study
boolean
C0020517 (UMLS CUI [1])
it is not possible to prescribe the study medication because it is contraindicated according to the summary of the product characteristic or according to the criteria of the physician responsible for patient
Item
it is not possible to prescribe the study medication because it is contraindicated according to the summary of the product characteristic or according to the criteria of the physician responsible for patient
boolean
C1301624 (UMLS CUI [1])
C0009488 (UMLS CUI [2])
Pregnancy
Item
Pregnancy
boolean
C0549206 (UMLS CUI [1])

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