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Clinical Trial

AcoArt Litos PCB Below-the-knee Global Trial

NCT: NCT06330493 · TERMINATED

NCT IDNCT06330493
StatusTERMINATED
Start Date2025-10-10
Completion2026-08-24
SponsorAcotec Scientific Co., Ltd (INDUSTRY)
First posted
Last updated

Brief Summary

The objective of this study is to assess whether efficacy of the AcoArt Litos PCB is superior and whether safety of AcoArt Litos PCB is noninferior to the control device (FDA cleared PTA Balloon Catheter) regarding treatment of obstructions in the infrapopliteal arteries (located distal to the P3 segment of the popliteal artery and extending to the tibiotalar joint) in patients presenting with chronic limb-threatening ischemia (CLTI)(Rutherford 4-5)

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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