New heart stent put to the test in 1,000 patients
NCT ID NCT06177743
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing a new heart stent called Coroflex ISAR NEO in 1,000 people with narrowed heart arteries. The goal is to see how safe and effective it is compared to other stents in everyday medical practice. Researchers will track major heart problems like death, heart attack, or the need for another procedure over one year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Coroflex ISAR NEO stent (a drug-coated mesh tube placed in heart arteries to keep them open)
- What this could lead to
- If successful, this could confirm that the Coroflex ISAR NEO stent is a safe and effective option for treating blocked heart arteries in everyday practice.
- What could go wrong
- This is an observational study, not a randomized trial, so results may be less definitive. Stents carry risks like blood clots or re-narrowing, and long-term outcomes are still being tracked.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Dec 2032
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients receiving Coroflex ISAR NEO stents.
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients ≥ 19 years old 2. Patients receiving Coroflex ISAR NEO stents. 3. The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethics Committee of the respective clinical site. Exclusion Criteria: 1. Patients with a mixture of other DESs 2. Terminal illness with life expectancy \<1 year. 3. Patients with cardiogenic shock
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
10 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Asan Medical Center
RECRUITINGSeoul, Songpa-gu, 138-736, South Korea
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Bucheon Sejong Hospital
RECRUITINGBucheon-si, South Korea
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Chonnam National University Hospital
NOT_YET_RECRUITINGGwangju, South Korea
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Inje University Ilsan Paik Hospital
NOT_YET_RECRUITINGIlsan, South Korea
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Myongji Hospital
RECRUITINGIlsan, South Korea
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Sejong Chungnam National University Hospital
RECRUITINGSejong, South Korea
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Seoul National University Boramae Medical Center
NOT_YET_RECRUITINGSeoul, South Korea
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The Catholic Univ. of Korea BUCHEON ST.Mary's hospital
RECRUITINGBucheon-si, South Korea
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The Catholic university of Korea, ST. Vincent's Hospital
RECRUITINGSuwon, South Korea
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Uijeongbu Eulji Medical Center
WITHDRAWNUijeongbu-si, South Korea
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Veterans Hospital
RECRUITINGDaegu, South Korea
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