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The Isthmus Logic Post Market Clinical Follow-up Study

Key facts

Who runs it
CID S.p.A.
Where
Italy1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
People taking part
37 people enrolled
Started
4 Sept 2023
Ended
22 May 2024
Type of study
Observational
Treatments tested
  • Isthmus Logic
Record updated
22 October 2026

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

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Who can take part

  • Patient has been implanted with at least one Isthmus Logic stent according to the indications described in the Instructions for Use (IFU)
  • Study device implantation date is at least one year (12 months) prior to the starting date of the retrospective anonymous data collection

Who cannot take part

  • Patients treated less than 12 months prior to study start

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

Isthmus Logic Carbostent™ is a CE-marked cobalt chromium stent with a bio inducer surface for the treatment of peripheral iliac artery disease.

Read full original descriptionShow less

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.

Treatments tested

  • Isthmus Logic

Data and sources

Registry record
Listed on ClinicalTrials.gov.
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.
Record updated
22 October 2026