At a glance
ClinicalIndex Comparison RecordN/ACompleted· 30 enrolled
Drug / intervention
Sigvaris Compreflex Inelastic Compression Wrapdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Effect of Inelastic Compression System on Quality of Life in People With Chronic Venous Insufficiency
In Brief
A clinical study evaluating Sigvaris Compreflex Inelastic Compression Wrap for Chronic Venous Insufficiency. Completed, enrolled 30 participants across 1 site.
Detailed Summary
The purpose of this protocol is to measure the effect of the use of an inelastic compression system (ICS) on quality of life (QOL) in patients with chronic venous insufficiency (CVI) who have demonstrated limited or no compliance with prescribed compression stockings or bandage wraps.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Venous Insufficiency
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedSep 2021
Enrollment StartNov 2021
Primary CompletionMay 2023
TodayJul 2026
First PostedSep 21, 2021
Enrollment StartNov 15, 2021
Primary CompletionMay 17, 2023
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 4.8 years ago
Interventions
Sigvaris Compreflex Inelastic Compression Wrapdevice
Compreflex compression system using wraps to apply compression of 30-40 mmHg.