Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions

NCT06779630 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to assess the safety and efficacy of the Orsiro® Mission 48- mm Sirolimus-Eluting Coronary Stent System in the treatment of subjects with atherosclerotic lesion(s) \>36 mm and ≤ 44 mm in length (by visual estimate) in the native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm. Patients enrolled in the United States will be followed for 2 years post index procedure with follow-up visits at 1, 6, 12 months and 2 years post index procedure. Patients enrolled outside of the United States will be followed through 5 years post index procedure with additional follow-up visits at 3 and 5 years post index procedure.

Conditions Studied

Interventions

  • DEVICE Orsiro Mission 48-mm Sirolimus-Eluting Coronary Stent System

Study Locations (15)

Texas

  • Baylor Scott & White The Heart Hospital - Dallas — Dallas
  • Ascension Texas Cardiovascular — Kyle

California

  • John Muir Medical Center — Concord

Kansas

  • Ascension Via Christi Hospitals Wichita — Wichita

New York

  • Columbia University Irving Medical Center/New York Presbyterian Hospital — New York

West Virginia

  • Charleston Area Medical Center — Charleston

Styria

  • Klinische Abteilung für Kardiologie, Medizinische Universität Graz — Graz

Vienna

  • Universitätsklinik für Innere Medizin II, Klinische Abteilung für Kardiologie, Medizinische Universität Wien — Vienna

Provence-Alpes-Côte d'Azur Region

  • Institut Arnault Tzanck — Saint-Laurent-du-Var

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2025-07-18
Est. Completion 2031-09
Phase NA

Sponsor

Teleflex

29 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06779630

The ClinicalTrials.gov registry entry for NCT06779630 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 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teleflex, which has 29 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Coronary Artery Disease appearing as the primary indexed condition, and to 1 intervention — of which Orsiro Mission 48-mm Sirolimus-Eluting Coronary Stent System 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: NCT06779630 reports 15 study locations spanning 14 distinct geographic areas — top geographies include Texas, California, Kansas. 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 NCT06779630 about?

NCT06779630 is a clinical study titled "Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions". The purpose of the study is to assess the safety and efficacy of the Orsiro® Mission 48- mm Sirolimus-Eluting Coronary Stent System in the treatment of subjects with atherosclerotic lesion(s) \>36 mm and ≤ 44 mm in length (by visual estimate) in the native coronary arteries with a reference vessel d...

What is the current status of trial NCT06779630?

This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2025-07-18. Estimated completion is 2031-09.

What conditions does trial NCT06779630 study?

This clinical trial studies the following conditions: Coronary Artery Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06779630?

The interventions under investigation include: Orsiro Mission 48-mm Sirolimus-Eluting Coronary Stent System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06779630?

This trial is sponsored by Teleflex, which has 29 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06779630 being conducted?

This trial has 15 study locations across California, Kansas, New York, Texas, West Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial