IVUS-Guided Sirolimus-Coated Balloon Versus Sirolimus-Eluting Stent for De Novo Large Vessel Lesions in ACS

Authors
Category Primary study
Registry of TrialsClinicalTrials.gov
Year 2026
Lesion preparation will be performed before randomization. Individuals with unsuccessfullesion preparation will be considered pre‐randomization failures and will not be assignedto either study arm. The reason for unsuccessful lesion preparation, the treatmentsubsequently received, and limited safety information through 48 hours after theprocedure will be documented for screening and safety oversight purposes only. Theseindividuals will not undergo protocol‐mandated follow‐up and will not be included in theefficacy or comparative safety analyses of the randomized trial.
Epistemonikos ID: b711c917d865deabfba19c191fb0e211504e71a8
First added on: Sep 01, 2026