Clinical Trials Directory

Trials / Unknown

UnknownNCT02808039

Is There a Transient Rebound Effect of Platelet Reactivity Following Cessation of Dual Antiplatelet Therapy With Ticagrelor - a Single Center Prospective Observational Trial

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Rabin Medical Center · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

to assess whether cessation of 12 months DAPT regimen containing Ticagrelor results in a hyperreactive phase of platelet function

Detailed description

the study will be composed of a cohort of patients , who completed 12 months of DAPT with Ticagrelor (standard recommended dose for ACS - 90 mg BID), did not experience any clinical or adverse event during this time period and are about to discontinue Ticagrelor. We intend to measure the platelet reactivity for each patient on 4 time points - prior to cessation of Ticagrelor (i.e. while still on DAPT) and 1,4 and 12 weeks post discontinuation of therapy. There will not be a control group.

Conditions

Interventions

TypeNameDescription
OTHERPlatelet reactivity testingassessment of platelet aggregation using the VerifyNow purinergic receptor P2Y, G-protein coupled, 12 (P2Y12) platelet function assay (Accumetrics, San Diego, California)

Timeline

Start date
2016-09-01
Primary completion
2017-04-01
First posted
2016-06-21
Last updated
2016-06-21

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02808039. Inclusion in this directory is not an endorsement.