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Feasibility of the InnoVein Valve and Delivery System for Chronic Venous Insufficiency

NCT04253301 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2021-09-17

No results posted yet for this study

Summary

This objective of this feasibility study is to evaluate the safety of the InnoVein Valve and Delivery System for treatment of chronic venous insufficiency.

Conditions

  • Chronic Venous Insufficiency

Interventions

DEVICE

InnoVein Valve Treatment

Subjects will have the InnoVein Valve implanted

Sponsors & Collaborators

  • InnoVein

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-15
Primary Completion
2022-02-15
Completion
2027-01-15

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04253301 on ClinicalTrials.gov