University of Oklahoma Health Sciences Center campus at the OU Vascular Center
Oklahoma City, Oklahoma, 73104, United States
NCT Number: NCT00954980
The overall objective will be to evaluate clinical predictors of outcomes in patients who undergo endovenous sclerotherapy for the treatment of varicose veins.
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Notify Me18 year and older
All sexes
Observational
Oklahoma City, Oklahoma, 73104, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: assessment will be at 1, 12, and 26 weeks.
Time frame: assessment will be at 1, 12, and 26 weeks
Time frame: assessment will be at 1, 12, and 26 weeks
Time frame: assessment will be at 1, 12, and 26 weeks
Time frame: assessment will be at 1, 12, and 26 weeks
Time frame: assessment will be at 1, 12, and 26 weeks
University of Oklahoma
Other
Evaluation of Clinical Characteristics of Endovenous Sclerotherapy of Varicose Veins
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