ID

42246

Beschrijving

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

Link

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

Trefwoorden

  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
Houder van rechten

AstraZeneca

Geüploaded op

14 april 2021

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Excerpt PLATO Acute coronary Syndrome NCT00391872

Study Termination

Study Termination
Beschrijving

Study Termination

Subject completed/prematurely terminated the study on
Beschrijving

Study complete date

Datatype

datetime

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

Study prematurely terminated

Datatype

boolean

Alias
UMLS CUI [1]
C2348570

Similar models

Study Termination

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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