EFS of the DUO System for Tricuspid Regurgitation (NCT05913908) | Clinical Trial Compass
RecruitingNot Applicable
EFS of the DUO System for Tricuspid Regurgitation
United States, Poland15 participantsStarted 2024-08-13
Plain-language summary
The study is an early feasibility study to measure individual patient clinical outcomes and effectiveness, evaluate the safety and function of the DUO Transcatheter Tricuspid Coaptation Valve System (DUO System).
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Presence of severe or greater tricuspid regurgitation as determined by the Echo Core Lab.
. Patient is symptomatic despite medical therapy.
. The local Site Heart Team determines the Patient is appropriate for transcatheter valve intervention.
. The Patient's anatomy is suitable in the judgment of the Patient Selection Committee.
. Age ≥18 years
. The Patient has been informed of the nature of the study and agrees to its provisions and has provided written Informed Consent.
Exclusion criteria
. Patient is currently participating in another clinical investigation that could affect the outcome of this trial.
. Any previous tricuspid valve intervention that would interfere with the placement of the investigational device.
. Moderate or greater tricuspid valve stenosis.
. Severe aortic, mitral and/or pulmonic valve stenosis and/or regurgitation
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.