Evaluation of Effectiveness and Safety of Synergy XD and Synergy Megatron™ Stent

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age19+
SponsorJung-min Ahn

About this trial

The objective of this study is to evaluate the effectiveness and safety of Synergy XD stent and Synergy Megatron™ Stent in the "real world" daily practice as compared with the other drug-eluting stents.

Eligibility criteria

Qualifiers

Patients ≥ 19 years old

Patients receiving Synergy XD stent(s) or Synergy Megatron™ stent(s).

The patient or guardian agrees to the study protocol and the schedule of clinical follow-up and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethics Committee of the respective clinical site.

Disqualifiers

Patients with a mixture of other drug-eluting stents (DESs)

Terminal illness with life-expectancy ≤1 year.

Patients with cardiogenic shock

Trial design

Treatments tested in this trial

  • Synergy XD stent or Synergy Megatron™ Stent

Treatment groups

2,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

Jung-min Ahn

Lead sponsor

Asan Medical Center

Sponsor institution

CardioVascular Research Foundation, Korea

Collaborator