ID

42247

Descrizione

Ticagrelor is a new, reversible binding, anti-platelet medication. Anti-platelet medications work to prevent the formation of blood clots. Ticagrelor is being developed as a treatment for patients with acute coronary syndrome (ACS). ACS is a term that is used to describe both heart attacks in progress or the imminent threat of a heart attack. ACS is usually caused by the formation of a blood clot in an artery that partially or totally blocks the blood supply to a portion of the heart muscle. Ticagrelor will be compared with clopidogrel to determine which drug, when either is used in conjunction with aspirin, is better at reducing deaths from vascular causes, future heart attacks and/or strokes in patients with ACS. https://clinicaltrials.gov/ct2/show/NCT00391872

collegamento

https://clinicaltrials.gov/ct2/show/NCT00391872

Keywords

  1. 28/11/15 28/11/15 -
  2. 14/04/21 14/04/21 - Ahmed Rafee, MD
  3. 15/04/21 15/04/21 - Ahmed Rafee, MD
Titolare del copyright

AstraZeneca

Caricato su

15 aprile 2021

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.

Excerpt PLATO Acute coronary Syndrome NCT00391872

Study Termination

Study Termination
Descrizione

Study Termination

Subject completed/prematurely terminated the study on
Descrizione

Study complete date

Tipo di dati

datetime

Alias
UMLS CUI [1]
C2983670
Was Subject's participation in the study prematurely terminated
Descrizione

Study prematurely terminated

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348570

Similar models

Study Termination

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Study Termination
Study complete date
Item
Subject completed/prematurely terminated the study on
datetime
C2983670 (UMLS CUI [1])
Study prematurely terminated
Item
Was Subject's participation in the study prematurely terminated
boolean
C2348570 (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