A Study Evaluating ClariVein With a Sclerosing Agent for the Treatment of Venous Insufficiency

Last updated: February 9, 2022
Sponsor: Vascular Insights, LLC
Overall Status: Terminated

Phase

2

Condition

Vascular Diseases

Deep Vein Thrombosis

Venous Thrombosis

Treatment

N/A

Clinical Study ID

NCT03311269
CL-001
  • Ages 18-80
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

VICARES is a prospective randomized, controlled, multi-center, double blind study treating venous insufficiency associated with incompetent saphenous veins with 1% and 3% Sodium Tetradecyl Sulfate (STS) solution utilizing the ClariVein system.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Adult patient with incompetent saphenous vein
  2. Saphenous vein reflux > 500ms (0.5s), as measured by duplex ultrasound
  3. One or more of patient reported symptoms related to the target vein: i.e., heaviness,achiness, swelling, throbbing or itching.
  4. Candidate for endovenous procedure

Exclusion

Exclusion Criteria:

  1. Arterial insufficiency demonstrated by a history of peripheral arterial disease (PAD)that would preclude the wearing of compression stockings
  2. Absence of a palpable pulse at posterior tibial or dorsalis pedis and anAnkle-Brachial Index (ABI) <0.6
  3. Multi-segmental axial deep venous reflux in at least two contiguous venous segments (e.g., femoral and popliteal) in the ipsilateral extremity
  4. Previous surgical or endovenous procedure in the treatment section of the target vein
  5. Previous superficial thrombophlebitis of the target saphenous vein with scarring inthe treatment section
  6. Pregnant or breastfeeding
  7. Known sensitivity or allergic response to Sodium Tetradecyl Sulfate (STS)
  8. Known high risk of thrombosis
  9. Known history of deep vein thrombus (DVT) or pulmonary embolism (PE), known history ofacute superficial vein thrombus, known hypercoagulable condition, post thromboticsyndrome
  10. Known history of anaphylaxis or presence of multiple severe allergies

Study Design

Total Participants: 19
Study Start date:
September 22, 2017
Estimated Completion Date:
March 27, 2020

Study Description

Approximately 50 subjects diagnosed with an incompetent saphenous vein will be randomized to either 1% STS or 3% STS solution delivered by the ClariVein system under ultrasound guidance.

Study duration for individual study patients, including follow-up visits, is anticipated to be approximately 16 weeks.

Connect with a study center

  • The Vascular Experts

    Darien, Connecticut 06820
    United States

    Site Not Available

  • Capitol Vein and Laser Centers

    Frederick, Maryland 21702
    United States

    Site Not Available

  • Southeastern Surgical Associates

    Hyannis, Massachusetts 02601
    United States

    Site Not Available

  • Englegwood Hospital and Medical Center

    Englewood, New Jersey 07631
    United States

    Site Not Available

  • Lake Washington Vascular, PLLC

    Bellevue, Washington 98004
    United States

    Site Not Available

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