Endovenous Ablation With and Without Polidocanol Endovenous Microfoam Treatment for Patients With Great Saphenous Vein Incompetence and Visible Varicosities
Completed · Phase 3 · Has a placebo group
Conditions studied: Great Saphenous Vein Incompetence, Visible Varicosities
In brief
Varicose veins are enlarged, noticeably bulging veins, which commonly occur in the legs and may cause discomfort. In this study, patients with varicose veins in the legs will be participating. The purpose of this research study is to evaluate the safety and effectiveness of two different doses of an investigational drug, Polidocanol Endovenous Microfoam (PEM) compared to vehicle (inactive solution) when used following an approved heat treatment in subjects with varicose veins.
Key facts
- Study ID
- NCT01197833
- Run by
- Boston Scientific Corporation
- People needed
- 117
- Starts
- 2010-09-01
- Expected to finish
- 2012-12-01
- Last updated by the study team
- 2021-04-21
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Incompetence of SFJ
- Patients who are candidates for ETA [laser or radiofrequency ablation (RFA)]
- Symptomatic varicose veins
- Visible varicose veins
- Ability to comprehend and sign an informed consent and complete study questionnaires in English
You may not qualify if…
- Patients who only have telangiectatic or reticular veins (Clinical Finding C1, as assessed by CEAP Classification of Venous Disorders)
- Patients who have active ulceration on the leg to be treated (Clinical Finding C6, as assessed by CEAP Classification of Venous Disorders)
- Leg obesity impairing the ability to access the vein to be treated and/or to apply post-procedure compression bandaging and stockings
- Ultrasonographic or other evidence of current or previous deep vein thrombosis or occlusion
- Deep venous reflux unless clinically insignificant in comparison to superficial reflux
- Peripheral arterial disease precluding the wearing of post-procedure compression bandaging and stockings
- Reduced mobility
- History of deep vein thrombosis, pulmonary embolism or stroke, including evidence of prior DVT on duplex ultrasound
- Major surgery, prolonged hospitalization or pregnancy within 3 months of screening
- Major co-existing disease (e.g. malignancy; pulmonary disease; renal or hepatic insufficiency; serious skin disease/condition that may compromise the ability of the patient to comply with the compression protocol, etc.)
- Known allergic response to polidocanol or heparin, including history of heparin-induced thrombocytopenia, and/or multiple allergic reactions
- Current alcohol or drug abuse
- Pregnant or lactating women
- Women of childbearing potential not using effective contraception
Where it is running
- Study site — Scottsdale, Arizona, United States
- Study site — Bradenton, Florida, United States
- Study site — Oak Brook, Illinois, United States
- Study site — North Tonawanda, New York, United States
- Study site — Stony Brook, New York, United States
- Study site — Charlotte, North Carolina, United States
- Study site — Kirkland, Washington, United States
Full record on ClinicalTrials.gov
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