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COMPLETED
NCT05616143

The Isthmus Logic Post Market Clinical Follow-up Study

Sponsor: CID S.p.A.

View on ClinicalTrials.gov

Summary

Isthmus Logic Carbostent™ is a CE-marked cobalt chromium stent with a bio inducer surface for the treatment of peripheral iliac artery disease. The aim of this post-market retrospective study protocl P22202 is to collect clinical data of patients treated with Isthmus Logic for the treatment of peripheral iliac artery disease in routine clinical practice. In order to obtain long-term follow-up data, the data collection will be limited to patients that have been treated with these devices at least 12 months prior to the study start.

Official title: A Cobalt Chromium Stent With a Bio Inducer Surface for the Treatment of Peripheral Iliac Artery Disease: Evaluation of Safety and Performance in Everyday Clinical Practice. The Isthmus Logic Post Market Clinical Follow-up Study.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

37

Start Date

2023-09-04

Completion Date

2024-05-22

Last Updated

2026-10-22

Healthy Volunteers

No

Interventions

DEVICE

Isthmus Logic

Patient implanted with Isthmus Logic stent for the treatment of peripheral iliac artery disease

Locations (1)

Ospedale San Raffaele

Milan, Italy