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Innoventric Trillium™ Stent Graft Early Feasibility Study (EFS)
NCT06212193 · View on ClinicalTrials.gov ↗
Study Summary
Early Feasibility Study to evaluate the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR).
Conditions Studied
Interventions
- DEVICE Trillium™
Study Locations (12)
New York
- Weill Cornell Medicine — New York
- Stony Brook Heart Institute — Stony Brook
California
- Cardiovascular Institute of Los Robles Health System — Thousand Oaks
Michigan
- Ascension St. John — Detroit
Minnesota
- Mayo Clinic Hospital (Rochester) — Rochester
Ohio
- The Christ Hospital — Cincinnati
Pennsylvania
- Lankenau Heart Institute — Philadelphia
Tennessee
- TriStar Centennial Medical Center — Nashville
Washington
- University of Washington Medical Center — Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2024-08-05 |
| Est. Completion | 2030-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06212193
The ClinicalTrials.gov registry entry for NCT06212193 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Innoventric, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Tricuspid Regurgitation appearing as the primary indexed condition, and to 1 intervention — of which Trillium™ is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06212193 reports 12 study locations spanning 11 distinct geographic areas — top geographies include New York, California, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06212193 about?
NCT06212193 is a clinical study titled "Innoventric Trillium™ Stent Graft Early Feasibility Study (EFS)". Early Feasibility Study to evaluate the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR).
What is the current status of trial NCT06212193?
This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2024-08-05. Estimated completion is 2030-08.
What conditions does trial NCT06212193 study?
This clinical trial studies the following conditions: Tricuspid Regurgitation, Tricuspid Regurgitation Functional. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06212193?
The interventions under investigation include: Trillium™ (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06212193?
This trial is sponsored by Innoventric, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06212193 being conducted?
This trial has 12 study locations across California, Michigan, Minnesota, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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