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STENTiT has successfully initiated first-in-human clinical trials (VITAL-IT 1) implanting its Resorbable Fibrillated Scaffold (RFS) in patients with below-the-knee chronic limb-threatening ischemia (CLTI). The RFS is fully bioresorbable, provides temporary support, and triggers natural artery regeneration. Early clinical results demonstrate restoration of blood flow with minimally invasive procedures; long-term patient monitoring is underway to assess durability and safety.
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