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NCT05677711

Safety and Efficacy of the Ultimaster Stent

Completed Last updated 25 November 2025
What this trial tests

trial testing ultimaster in Coronary Artery Disease in 204 participants. Completed in 3 January 2025.

Timeline
20 July 2021
Primary endpoint
24 September 2024
3 January 2025

Quick facts

Lead sponsorYonsei University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment204
Start date20 July 2021
Primary completion24 September 2024
Estimated completion3 January 2025
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Yonsei University

Who can join

19 and older, any sex, with Coronary Artery Disease or Drug-eluting Stents. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Durable polymer was considered to be the cause of a chronic inflammatory response that leadas to impaired endothelialization of the stent strut and subsequently increases the risk of stent thrombosis. Ultimaster stent (Ultimaster, Terumo Corporation, Tokyo, Japan) are thin strut, silorimus-eluting, biodegradable copolymer to completely degrade over 3-4 months.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other Yonsei University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05677711.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing