Trials / Not Yet Recruiting
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.