ID

12602

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT01301313

Keywords

  1. 04/12/2015 04/12/2015 -
Caricato su

4 de dezembro de 2015

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Acute Heart Failure NCT01301313

Eligibility Acute Heart Failure NCT01301313

Inclusion Criteria
Descrizione

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.
Descrizione

Informed consent

Tipo di dati

boolean

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

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

Tipo di dati

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.
Descrizione

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

Tipo di dati

boolean

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

Exclusion Criteria

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

Informed consent denied

Tipo di dati

boolean

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

cardiomyopathy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0878544
aortic stenosis
Descrizione

aortic stenosis

Tipo di dati

boolean

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

allergy

Tipo di dati

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
Descrizione

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

Tipo di dati

boolean

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

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0549206

Similar models

Eligibility Acute Heart Failure NCT01301313

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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])

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial