Clin2
NCT06710210Possibly a fitRecruiting

Hybrid scaffold-balloon vs standard stent for long blockages

Coronary Artery DiseaseDiffuse Coronary Artery DiseasePercutaneous Coronary Intervention (PCI)

Part of Heart & circulation clinical trials.

This trial tests a new way to treat long, narrow blockages in heart arteries. Instead of using a standard permanent metal stent, doctors will combine a temporary scaffold with a special balloon that releases medication. The goal is to see if this approach works as well as or better than the usual metal stent.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
150 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be at least 18 years old.
  • You must have a long (over 40 mm) narrowed area in one or more of your heart arteries.
  • You must be stable enough for a heart procedure (not in severe shock).
  • You cannot have had a stent placed in that same heart artery in the last 12 months.
  • You must be able to take two blood thinners (aspirin plus clopidogrel, prasugrel, or ticagrelor) for at least 6 months.
  • You cannot have a known allergy to the components of the trial devices or blood thinners.

View the official record on ClinicalTrials.gov

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Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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