| Eligibility |
Inclusion Criteria:
- 1. 18 years of age or older;
- 2. Symptomatic CVI subjects, Clinical Etiological Anatomical Pathophysiological (CEAP)
classification 4 to 6;
- 3. Failed at least 6 months of conservative therapy at some point during the course of
their CVI management (symptoms not adequately resolved or patient non-compliant/unable
to tolerate);
- 4. Willing and able to sign the approved informed consent form (ICF);
- 5. Willing to comply with follow-up evaluations and protocols;
- 6. Deep system venous reflux characterized by >1 second reflux time in two contiguous
vein segments (vein segments defined as: proximal femoral, distal femoral, and
popliteal), as assessed by DUS with patient in the standing position;
- 7. Presence of at least two potential target sites within the target vessel, which is
defined as a segment within the femoral or popliteal vein that is:
- not less than 7mm in luminal diameter, and
- not more than 11mm in luminal diameter, and
- at least 3cm long (two target sites in a row must be spaced at least 1cm apart),
and
- absent severe obstructive features such as thrombus, synechiae, natural valves,
major tributaries (valves can be formed opposite tributaries) or severe
heterogeneous fibrotic changes of the vessel wall which, in the Investigator's
opinion, would preclude formation of a valve, as preliminary assessed by DUS, and
then by IVUS, while the vein is under physiologically appropriate hemodynamic
pressure, with IVUS being the definitive modality.
- 8. In the Investigator's opinion, the subject is a good candidate for treatment with
the BlueLeaf System based on their symptoms, quality of life, anatomy, and the
likelihood of benefit from continued conservative therapy.
Exclusion Criteria:
- 1. Untreated significant superficial venous incompetence within 30 days of screening
which, in the opinion of the Investigator, may be the primary source of existing
symptoms;
- 2. A competent vein valve in any vein segment through which the device is likely to be
inserted, as assessed by DUS (<1 second reflux time) or with contrast venography
(Investigator's opinion);Deep venous intervention (includes stenting) in the target
limb or outflow vessels within 90 days of consent;
- 3. Deep venous intervention (includes stenting) in the target limb or outflow vessels
within 90 days of consent
- 4. Significant peripheral arterial disease with an ankle-brachial index of <0.70 or
with incompressible vessels;
- 5. Contraindications to all protocol specified anticoagulation options;
- 6. Known and uncontrolled hypercoagulopathy (i.e. hypercoagulopathy that cannot be
adequately managed/controlled with medication);
- 7. Acute deep venous thrombosis (DVT) within 6 months of consent;
- 8. Comorbidity risks or other concerns (e.g. recent cancer) which, in the opinion of
the Investigator, limit longevity or likelihood of complying with the protocol and its
prescribed follow up or would preclude the patient from open surgery in the event of a
complication requiring surgical intervention (e.g. severe vein laceration);
- 9. General contraindications to local, regional or general anesthesia required for the
index procedure;
- 10. NYHA Class III or IV heart failure;
- 11. Active systemic infection;
- 12. Women on long-term oral contraceptives;
- 13. Subject is enrolled in another clinical study that, in the opinion of the
Investigator, may conflict with this study or compromise study results;
- 14. Invasive surgical procedure within the last 90 days that in the Investigator's
opinion would interfere with the study procedure or results;
- 15. History of stroke within the last 6 months;
- 16. Flow-limiting venous outflow obstruction central to the intended target sites,
defined by a common femoral vein duplex exam found to have a continuous waveform
without respiratory variation or a 50% or greater reduction in luminal cross-sectional
area on IVUS;
- 17. Inadequate flow into or through the target vessel (Investigator's opinion);
- 18. Anatomy that does not support proper device access of the treatment vein through
the ipsilateral common femoral or femoral vein;
- 19. Luminal diameter <7 mm between the vein access site and the intended treatment
site, as assessed by IVUS, while the vein is under physiologically appropriate
hemodynamic pressure;
- 20. A competent vein valve in any vein segment through which the device is likely to
be inserted (common femoral or femoral vein)
- 21. Chronic renal insufficiency with creatinine level of =2mg/dL;
- 22. Hemoglobin level <9.0 mg/dL;
- 23. Platelet count <50,000 or >1,000,000 per mm3;
- 24. Total white blood cell count <3,000/mm3;
- 25. Pregnant or lactating female; positive pregnancy test, women of childbearing
potential must be tested;
- 26. Non-ambulatory patients;
- 27. Patients with a history of right heart failure occurring as a consequence of, for
example, biventricular failure, intrinsic pulmonary disease, chronic thromboembolic
pulmonary hypertension, and other etiologies that result in elevated right-sided
pressures.
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