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Clinical Trials/NCT06264843
NCT06264843RecruitingNot Applicable

Open, Prospective, Multicentre Study Addressing the Immediate Benefits and the Prognostic Value of Intraoperative Completion Control Following Infrainguinal Bypass Surgery in Chronic Limb-Threatening Ischemia (CLTI) Patients

Medistim ASA1 site in 1 country450 target enrollmentStarted: November 14, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
450
Locations
1
Primary Endpoint
Primary graft patency rate

Study Overview

Brief Summary

The goal of the study is to identify and validate flow measurement and ultrasound images in patients undergoing vein bypass surgery below-knee and above ankle

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Chronic Limb-Threatening Ischemia as defined by presence of Peripheral Artery Disease (PAD) in combination with rest pain, gangrene, or a lower limb ulceration>2 weeks duration (ref Global Guidelines)
  • •Atherosclerotic infra-popliteal PAD
  • •Adequate distal anastomotic target (crural, tibial or popliteal below the knee with one single run-off) between knee and ankle distal to the stenotic/occluded segment.
  • •Available autogenous vein conduit based on preoperative vein mapping.
  • •Understand the nature of the procedure and willingness to comply with protocol. Attend follow-up appointments and provide written informed consent.

Exclusion Criteria

  • •Bypass with artificial conduit or cryopreserved allografts
  • •Bypass for non-atherosclerotic lesions
  • •Life-expectancy less than 2 years
  • •Any psychological, developmental, physical or emotional disorder that the investigator believes would interfere with surgery or follow-up.
  • •Any condition that the investigator believes should exclude participation.
  • •Excessive risk for adverse events during open surgery as judged by the investigator.

Arms & Interventions

Patency of lower extremity vein bypass grafts

Primary patency of lower extremity vein bypass grafts at one year

Intervention: MiraQ with Transit-Time Flow Measurement (TTFM) and L15 High Frequency Ultrasound (HFUS) probes (Device)

Outcomes

Primary Outcomes

Primary graft patency rate

Time Frame: at 1 year

Freedom from any repeat graft intervention, graft thrombosis, or clinically significant stenosis (\>70% by either Duplex criteria or angiographic imaging) in the bypass

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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