Viewing Study NCT01642966



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Last Modification Date: 2024-10-26 @ 10:54 AM
Study NCT ID: NCT01642966
Status: COMPLETED
Last Update Posted: 2013-01-23
First Post: 2012-07-12

Brief Title: Differential Effect of Ticagrelor Versus Prasugrel on the Adenosine-induced Coronary Vasodilatory Responses in Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
Sponsor: University of Patras
Organization: University of Patras

Study Overview

Official Title: Differential Effect of Ticagrelor Versus Prasugrel on the Adenosine-induced Coronary Vasodilatory Responses in Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
Status: COMPLETED
Status Verified Date: 2013-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a prospective randomized single-blind investigator-initiated crossover study Patients with Acute Coronary Syndrome ACS subjected to percutaneous coronary intervention PCI are randomized after informed consent in a 11 ratio to either ticagrelor 90mg x2 or prasugrel 10mg x1 for 15 days At Day 15 2 days coronary diastolic blood flow velocity in left anterior descending artery LAD is evaluated at baseline bCBFV and under 2 min adenosine infusions maximal diastolic CBFV- maxCBFV at gradually increasing doses of 50μgkgmin 80μgkgmin 110μgkgmin and 140μgkgmin with at least 5 min recovery intervals between infusions A crossover directly to the alternate treatment is performed followed by the same evaluation at Day 302 days
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None