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Completed No phase listed Observational

A U.S Post Approval Study Evaluating the SYNERGY XLV (MEGATRON) Stent System

ClinicalTrials.gov ID: NCT04807439

Public ClinicalTrials.gov record NCT04807439. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 11, 2026, 4:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A U.S. Post-Approval Study of the SYNERGYTM Everolimus-Eluting Platinum Chromium Coronary Stent System Evaluating the SYNERGY XLV (MEGATRON) Stent System

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a post-market, standard of care, real-world observational study to assess the clinical outcomes of the SYNERGY XLV (MEGATRON) Coronary Stent System for the treatment of subjects with atherosclerotic lesion(s) ≤ 28 mm in length (by visual estimate) in native coronary arteries ≥3.50 mm to ≤5.00 mm in diameter (by visual estimate). This Post Approval study is a cohort associated with the Evolve 4.5/5.0 (SYNERGY LV) Post Approval Study, which is registered under ClinicalTrials.gov ID: NCT03875651.

Study identification

NCT ID
NCT04807439
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Boston Scientific Corporation
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 13, 2021
Primary completion
Aug 18, 2022
Completion
Aug 17, 2023
Last update posted
Oct 22, 2023

2021 – 2023

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Yale University New Haven Connecticut 06520
Clearwater Cardiovascular Consultants Clearwater Florida 33756
Beth Israel Deaconness Medical Center Boston Massachusetts 02215
North Kansas City Hospital Kansas City Missouri 64116
Wake Medical Center Raleigh North Carolina 27607
Oregon Health Sciences University Portland Oregon 97239
Baylor Heart and Vascular Hospital Dallas Texas 75226
Inova Fairfax Hospital Fairfax Virginia 22042

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04807439, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 22, 2023 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04807439 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →