Information:
Fel:
ID
12602
Beskrivning
Efficacy and Safety of Levosimendan in Severe Acute Heart Failure in Critical Children; ODM derived from: https://clinicaltrials.gov/show/NCT01301313
Länk
https://clinicaltrials.gov/show/NCT01301313
Nyckelord
Versioner (1)
- 04/12/2015 04/12/2015 -
Uppladdad den
4 décembre 2015
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Acute Heart Failure NCT01301313
Eligibility Acute Heart Failure NCT01301313
- StudyEvent: Eligibility
Similar models
Eligibility Acute Heart Failure NCT01301313
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
C0264714 (UMLS CUI [2])
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])
C0009488 (UMLS CUI [2])
Pregnancy
Item
Pregnancy
boolean
C0549206 (UMLS CUI [1])