No phaseRecruiting

Noninferiority Trial Of Sirolimus With Ascorbic Acid Versus Everolimus in All-comers (NOVA)

Sponsor
Jung-min Ahn (Academic or other)
Enrolment
2,034 planned
Conditions
Coronary Artery Disease
Interventions
Sirolimus-Ascorbic Acid Eluting Stent; Everolimus-Eluting Stent
Ages
adults, older adults
Registry
NCT07566091

Full record on ClinicalTrials.gov

From the registry

The objective of this study is to demonstrate the primary hypothesis that, in patients with chronic and acute coronary syndromes requiring percutaneous coronary intervention (PCI), the novel sirolimus-ascorbic acid eluting stent (D+Storm Novonix) is non-inferior to the standard treatment, the everolimus-eluting stent (Synergy XD), with respect to the incidence of target lesion failure (TLF) at 1 year after treatment, where TLF is defined as a composite of cardiovascular death, target vessel myocardial infarction, and clinically driven target-lesion revascularization.

Primary outcomes

  • The event rate of Target Lesion Failure

History

  1. Study completion expected

  2. Primary completion expected

  3. Last registry update

  4. Started

  5. Registered