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Not Yet RecruitingNCT07140133

Dual Anti-Platelet Optimized Stent for High Bleeding Risk Patient

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
1,200 (estimated)
Sponsor
University Hospital, Grenoble · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

High risk of bleeding (HBR) is a determining factor for the duration of dual antiplatelet therapy (DAPT). Recent studies have shown that the use of one-month DAPT is beneficial in terms of ischemic as well as hemorrhagic events, particularly in HBR patients, compared with longer DAPT. European guidelines therefore authorize one-month DAPT in HBR patients presenting even an acute coronary syndrome. The HT Supreme Drug Coated Coronary Stent System (HT Supreme DES) is designed to promote reendothelialization as quickly as possible. That's why the stent is called "HT" Supreme, with "HT" standing for "Healing Targeted", enabling a DAPT of just 1 month in all-comers HBR patients. Thanks to these features, the investigators aim to demonstrate ischemic and hemorrhagic complication rates lower than those found in the literature with other stent.

Conditions

Timeline

Start date
2025-09-01
Primary completion
2027-09-01
Completion
2027-09-01
First posted
2025-08-24
Last updated
2025-08-24

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07140133. Inclusion in this directory is not an endorsement.

Dual Anti-Platelet Optimized Stent for High Bleeding Risk Patient (NCT07140133) · Clinical Trials Directory