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Clinical trial

Prospective Multi-Center Randomized Controlled Trial to Evaluate the Safety and Efficacy of AcoArt Litos Paclitaxel Coated Percutaneous Transluminal Angioplasty (PTA) Balloon Versus Non-Coated Standard Balloon Angioplasty for the Treatment of Infrapopliteal Obstructions in Patients With Chronic Limb-Threatening Ischemia

NCT06330493 is registered in ClinicalTrials.gov with Acotec Scientific Co., Ltd as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Prospective Multi-Center Randomized Controlled Trial to Evaluate the Safety and Efficacy of AcoArt Litos Paclitaxel Coated Percutaneous Transluminal Angioplasty (PTA) Balloon Versus Non-Coated Standard Balloon Angioplasty for the Treatment of Infrapopliteal Obstructions in Patients With Chronic Limb-Threatening Ischemia
Lead sponsor
Acotec Scientific Co., Ltd
Phase
Not applicable
Overall status
Terminated
Start date
October 10, 2025
Completion date
August 24, 2026
Enrollment
75 (actual)
Sites
18

Conditions

As the registry lists them; a condition with its own page is linked.