Community RCT of the Effectiveness of Two Compression Bandaging Technologies
Venous Ulcer
About this trial
This is an interventional treatment trial for Venous Ulcer focused on measuring leg ulcer, compression, bandage, APBI, venous insufficiency
Eligibility Criteria
Inclusion Criteria: clinical presentation of venous insufficiency leg ulcer equal to or larger than 0.7 cm in any one dimension ulcer a minimum duration of 1 week ankle brachial pressure index equal to or greater than 0.80 participant can provide written consent participant can communicate in English, or translation available participant 18 years or over Exclusion Criteria: diagnosed with Diabetes Mellitus - insulin dependent or participant on oral hypoglycemics participants who failed to improve over a 3-month period after being treated with either the SS or 4-layer compression bandaging system prior to the trial previous trial patients (ie individuals previously enrolled in the study but now have recurrence or a new ulcer) symptoms of cognitive impairment noted
Sites / Locations
- Winnipeg Regional Health Authority
- Nursing Practice Solutions
- VON Hamilton Branch
- Saint Elizabeth Health Care
- Kingston Chronic Wound Clinic
- ParaMed Health Services
- ET Now
- Carefor
- ParaMed Health Services
- St. Joseph's Care Group
- St. Michael's Hospital
- ParaMed Home Health Care
- Comcare Health
- Ostomy and Wound Care Centre
- Saskatoon Health Region Home Care
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
1
2
Clients randomized to short-stretch bandaging application
Clients randomized to four-layer bandaging application