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Trials / Recruiting

RecruitingNCT06301776

A Prospective, Experimental, Multicenter, Open-label, Randomized, Controlled Trial of 3-month Dual Antiplatelet Therapy Followed by Ticagrelor Versus 6-month Dual Antiplatelet Therapy Followed by Ticagrelor After Implanting Bridge

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
560 (estimated)
Sponsor
The Fourth Affiliated Hospital of China Medical University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To compare the incidence of the composite endpoints of non-fatal ischaemic stroke, transient ischaemia (TIA) and all-cause mortality at 12-month follow-up after implantation of Bridge for the treatment of symptomatic vertebral artery stenosis in subjects who had been taking different durations of dual-antiplatelet therapy (3 vs 6 months) and ticagrelor monotherapy.

Conditions

Interventions

TypeNameDescription
DRUGTicagrelorTo compare the safety and efficacy of different DAPT duration combined with ticagrelor monotherapy.

Timeline

Start date
2023-12-05
Primary completion
2025-12-31
Completion
2026-06-30
First posted
2024-03-08
Last updated
2024-03-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06301776. Inclusion in this directory is not an endorsement.

A Prospective, Experimental, Multicenter, Open-label, Randomized, Controlled Trial of 3-month Dual Antiplatelet Therapy (NCT06301776) · Clinical Trials Directory