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Evaluation of Endovenous Sclerotherapy for Treatment of Varicose Veins

Evaluation of Clinical Characteristics of Endovenous Sclerotherapy of Varicose Veins

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00954980
Enrollment
100
Registered
2009-08-07
Start date
2009-05-31
Completion date
2016-07-31
Last updated
2016-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Varicose Veins

Keywords

Varicose Veins, Superficial Thrombophlebitis, Deep Vein Thrombosis, Ulceration, leg pain, leg swelling

Brief summary

The overall objective will be to evaluate clinical predictors of outcomes in patients who undergo endovenous sclerotherapy for the treatment of varicose veins.

Detailed description

A prospective cohort study of patients who undergo endovenous sclerotherapy over 2 years. There are no deviations in usual clinical assessment and care of patients seeking varicose vein treatment. The purpose of this protocol is only to collect clinical and biomarker information related to this standard treatment.

Interventions

None listed

Sponsors

University of Oklahoma
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Clinical diagnosis of varicose veins

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Frequency of obliteratin (total or partial) of injected varicosity.assessment will be at 1, 12, and 26 weeks.
Improvement in venous stasis symptoms.assessment will be at 1, 12, and 26 weeks
Change in quality of life.assessment will be at 1, 12, and 26 weeks
Associations between clinical outcomes and biomarkers.assessment will be at 1, 12, and 26 weeks

Secondary

MeasureTime frame
Recurrence of varicosities.assessment will be at 1, 12, and 26 weeks
Adverse events reported following procedure.assessment will be at 1, 12, and 26 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026