Principal Investigator
Enrollment Status
Clinical Trial ID
Clinical Trial 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.
Phase
N/A
Funding Agency/Sponsor
Other
Disease
Other
Enrollment Eligibility
Inclusion Criteria:
- Subject is age 18 or older, able and willing to provide consent and agrees to comply
with the study procedures
- Subject must have chronic venous insufficiency of stages C3, C4, or C5 according to
the Clinical-Etiological-Anatomical-Pathophysiological (CEAP) classification system
- Not compliant with their currently prescribed compression system
Exclusion Criteria:
- Active malignancy other than non-melanoma skin cancer
- Study ulcer suspicious for cancer
- Subjects who are pregnant and/or breastfeeding
- In the opinion of the PI the subject cannot comply with study procedures