ID

42247

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

15 april 2021

DOI

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Licentie

Creative Commons BY 4.0

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Excerpt PLATO Acute coronary Syndrome NCT00391872

Section Investigational Products

Investigational product: AZD6140/placebo
Beschrijving

Investigational product: AZD6140/placebo

Alias
UMLS CUI-1
C1608718
First dose
Beschrijving

AZD6140 first dose

Datatype

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C1608718
Last dose
Beschrijving

AZD6140 last dose

Datatype

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C1608718
Investigational product: Clopidogrel/placebo
Beschrijving

Investigational product: Clopidogrel/placebo

Alias
UMLS CUI-1
C0070166
First dose
Beschrijving

Clopidogrel first dose

Datatype

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C0070166
Last dose
Beschrijving

Clopidogrel last dose

Datatype

datetime

Alias
UMLS CUI [1,1]
C3173975
UMLS CUI [1,2]
C0070166
Additional Dose of Investigational Products
Beschrijving

Additional Dose of Investigational Products

Interruption of Investigational Products
Beschrijving

Interruption of Investigational Products

Subject Drug Accountability
Beschrijving

Subject Drug Accountability

Similar models

Section Investigational Products

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Investigational product: AZD6140/placebo
C1608718 (UMLS CUI-1)
AZD6140 first dose
Item
First dose
datetime
C3173975 (UMLS CUI [1,1])
C1608718 (UMLS CUI [1,2])
AZD6140 last dose
Item
Last dose
datetime
C3173975 (UMLS CUI [1,1])
C1608718 (UMLS CUI [1,2])
Item Group
Investigational product: Clopidogrel/placebo
C0070166 (UMLS CUI-1)
Clopidogrel first dose
Item
First dose
datetime
C3173975 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
Clopidogrel last dose
Item
Last dose
datetime
C3173975 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
Item Group
Additional Dose of Investigational Products
Item Group
Interruption of Investigational Products
Item Group
Subject Drug Accountability

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