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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of Polidocanol Injectable Foam for the Treatment of Saphenofemoral Junction (SFJ) Incompetence

ClinicalTrials.gov ID: NCT01072877

Public ClinicalTrials.gov record NCT01072877. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 12:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Blinded, Multicenter Study to Evaluate the Efficacy and Safety of Polidocanol Injectable Foam 0.5%, 1.0%, or 2.0% Compared to Vehicle for the Treatment of Saphenofemoral Junction (SFJ) Incompetence

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 three different concentrations of an investigational drug, polidocanol injectable foam compared to vehicle (inactive solution) in treating the symptoms and appearance of varicose veins.

Study identification

NCT ID
NCT01072877
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boston Scientific Corporation
Industry
Enrollment
279 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2010
Primary completion
Nov 30, 2011
Completion
Oct 31, 2012
Last update posted
Apr 20, 2021

2010 – 2012

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Not listed Laguna Hills California 92653
Not listed San Diego California
Not listed Washington D.C. District of Columbia 20007
Not listed Aventura Florida 33180
Not listed Bradenton Florida 34209
Not listed Oakbrook Terrace Illinois 60181
Not listed Ann Arbor Michigan 48109
Not listed Kalamazoo Michigan 49009
Not listed Hartsdale New York 10530
Not listed New York New York 10016
Not listed North Tonawanda New York 14120
Not listed Stony Brook New York 10530
Not listed Charlotte North Carolina 28207
Not listed Durham North Carolina 27705
Not listed Winston-Salem North Carolina 27157
Not listed Toledo Ohio 43606
Not listed Bend Oregon 97701
Not listed Clarksville Tennessee 37040
Not listed Kirkland Washington 98034
Not listed Spokane Washington 99204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01072877, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 20, 2021 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01072877 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →