A Feasibility Study of the ReLeaf Catheter System

Chronic Venous Insufficiency Clinical Trial

— ReLeaf  

Official title:

A Feasibility Study of the InterVene ReLeaf Catheter System in the Creation of Tissue Leaflets in the Femoral and/or Popliteal Vein

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02462096
• Other study ID #: CLP-0001
• Status: Terminated
• Phase: N/A
• First received: May 26, 2015
• Last updated: March 26, 2018
• Start date: September 9, 2015
• Est. completion date: June 5, 2017

Study information

• Verified date: March 2018
• Source: Intervene, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is designed to evaluate the safety and technical feasibility of the ReLeaf Catheter System in the creation of one or more tissue leaflets in the femoral and/or popliteal vein in subjects with chronic venous insufficiency and who meet the protocol entry criteria.

Description:

The ReLeaf catheter system is intended for the creation of tissue leaflets in the deep veins where existing valve structures are no longer healthy and effectively moving blood.

This study aims to treat subjects with a documented history of symptomatic chronic venous insufficiency in whom compression therapy for at least 6 months, combined with superficial venous and/or perforator surgery have failed to obtain clinical improvement.

This clinical trial is designed to evaluate the safety and technical feasibility of the ReLeaf Catheter System in the creation of one or more tissue leaflets in the femoral and/or popliteal vein in subjects with chronic venous insufficiency and who meet the protocol entry criteria.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: June 5, 2017
• Est. primary completion date: October 8, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• History of symptomatic chronic venous insufficiency subjects, clinical category CEAP 3 or greater.

• History of failed compression therapy (of at least 6 months), combined with superficial venous or perforator surgery.

• Femoral and/or popliteal venous reflux of = 1.0 seconds.

• Deep system reflux with Kistner classification grade 2 or higher.

• 18 years of age or older at the time of consent.

• Willing and able to sign the Ethics Committee (EC) approved informed consent form.

• Willing to comply with follow-up evaluations and protocols.

Exclusion Criteria:

• In the Investigator's opinion, venous outflow obstruction that would inhibit adequate flow away from valve site.

• Obstructive features in the femoral or popliteal vein below the proposed tissue leaflet creation site, which, in the Investigator's opinion, will not allow for sufficient blood flow to the tissue leaflet creation site.

• Deep venous system intervention within 6 months of consent.

• Obstructive features or irregularly small luminal diameter in the femoral vein which, in the opinion of the Investigator, will prohibit access to a tissue leaflet creation site.

• Prior deep vein valve surgical intervention in the ipsilateral limb.

• Ankle arthrodesis with secondary muscle atrophy or severely limited ambulation.

• Limb-threatening circulatory compromise.

• Contraindications to anticoagulation therapy that cannot be medically controlled.

• History of symptomatic pulmonary embolism.

• Acute venous thromboembolism within 3 months of consent.

• Comorbidity risks which, in the opinion of the Investigator, limit longevity or likelihood of complying with protocol follow up.

• General contraindications to surgery or the use of anesthesia.

• Uncontrolled heart failure, or NYHA Class III or IV heart failure.

• Open Cardiac surgery (e.g. ventriculotomy, atriotomy) within the past 6 months of consent (Interventional procedures such as stenting or PTCA do not apply.)

• Chronic Kidney Disease with creatinine level of 2mg/dL or higher.

• Active systemic infection or sepsis.

• Pregnant or lactating (positive pregnancy test, women of childbearing potential must be tested).

• Appropriate vascular access is precluded.

• Subject is enrolled in any other clinical study that, in the opinion of the Investigator, may conflict with this study or compromise study results.

• Subject is considered at high risk for non-compliance with the protocol (e.g., inaccessible for follow-up).

• Other invasive surgical procedure within the last 90 days that in the Investigator's opinion would interfere with the study procedure or results.

• History of stroke within the last 6 months.

• Subject is incarcerated or will be incarcerated during the course of the study.

• Untreated significant superficial venous incompetence

Related Conditions & MeSH terms

• Chronic Venous Insufficiency
• Venous Insufficiency

Intervention

Device:
• ReLeaf
The ReLeaf catheter is expected to enable a physician to create tissue leaflets that, in turn, generate a valve effect in the deep veins of the legs.

Locations

Country	Name	City	State
New Zealand	Auckland City Hospital	Auckland

Sponsors (1)

Lead Sponsor	Collaborator
Intervene, Inc.

Country where clinical trial is conducted

New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Efficacy	Subsequent efficacy of the treatment following successful creation of the tissue leaflet(s). This will be measured through an assessment of tissue leaflet creation and the tissue leaflets ability to impact blood flow over the course of time.	Day 365
Other	Durability	Long-term durability of the tissue leaflet(s). Confirmation of tissue leaflet existence over time will be used to assess the durability of the tissue leaflet.	Day 365
Other	Long-term Safety (Long-term safety will be measured by freedom from SAEs directly attributable to the study device)	Further long-term safety data will be collected, analyzed and reported through the end of the study. Long-term safety will be measured by freedom from SAEs directly attributable to the study device.	Day 365
Primary	Technical Feasibility	Technical feasibility will be evaluated as the ability of the ReLeaf Catheter System to access the target site and successfully modify tissue as confirmed by, and in the opinion of, the Investigator. Successful target site access and confirmed tissue modification will be used as a measure of technical feasibility.	Day 0
Primary	Safety (The number of SAEs directly attributable to the study device will be used as a measure of safety)	Safety will be evaluated as freedom from serious adverse events directly attributed to the investigational device. The number of SAEs directly attributable to the study device will be used as a measure of safety.	Day 30