Can a dissolving stent coating beat a permanent one for blocked arteries?
NCT ID NCT01516723
First seen Aug 18, 2026 · Last updated Aug 18, 2026
Summary
This trial compares two types of drug-eluting stents—tiny mesh tubes that prop open arteries—in people with completely blocked coronary arteries. One stent uses a coating that dissolves over time (bioresorbable polymer) to release the drug sirolimus, while the other has a permanent coating that releases everolimus. The goal is to see which stent better keeps the artery open and reduces the chance of re-narrowing, measured by how much the vessel narrows again at 9 months. Participants are adults with a blocked artery that has been successfully reopened, and the study randomly assigns them to receive one of the two stents.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- Two types of drug-eluting stents: a hybrid sirolimus-eluting stent with a bioresorbable polymer (ORSIRO) and an everolimus-eluting stent with a durable polymer (XIENCE PRIME), both used to reopen totally blocked coronary arteries.
- What this could lead to
- If the bioresorbable-polymer stent works as well or better, it could reduce the risk of late stent complications and improve long-term outcomes for people with completely blocked coronary arteries.
- What could go wrong
- This is a mid-sized trial, and the outcome is measured at 9 months—longer-term effects, such as very late stent thrombosis, may not be fully captured. Also, results may not apply to all patients with coronary artery disease.
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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.
Contacts and locations
Locations
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AMC
Amsterdam, Amsterdam, 1105AZ, Netherlands
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AZ Middelheim
Antwerp, Antwerpen, 2020, Belgium
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Catharina Ziekenhuis
Eindhoven, Eindhoven, 5602ZA, Netherlands
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St Antonius Hospital
Nieuwegein, 3435CM, Netherlands
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