The goal of this open-label, post-market clinical follow-up study is to demonstrate the safety and effectiveness of HealiAid Collagen Wound Dressing in patients classified into different types of wounds: venous ulcers, bedsores, diabetic foot wounds and burn wounds. The main questions it aims to answer are: 1. The wound healing which was defined as the percentage of area change. 2. The duration of wound healing. 3. The granulation tissue growth of the wound. 4. The wound exudate. 5. Safety Indicators of which incidences after treatment. HealiAid will be applied to eligible subjects who will later be followed up for 12 weeks.
An open-label study will be performed in single center to monitor about 6 patients in each types of wounds: venous ulcers, bedsores, diabetic foot wounds and burn wounds, totally 24 patients, after the treatment of using HealiAid Collagen Wound Dressing (MAXIGEN BIOTECH INC., Taiwan) directly on the wound sites. Follow-up visits will be at 1, 2, 4, 8 and 12(if needed) weeks after the treatment. The primary endpoint of this study was the area percentage of healed wound at the 8-week post-treatment interval, which is also considered as the healing condition of the wound. The secondary endpoints of this study were included the duration of wound healing, granulation tissue growth, wound exudate, and the incidence of safety events. T-test or Wilcoxon rank-sum test will be used to test for the differences between baseline and each visit. Statistical significance was established at p \< 0.05. The actual enrollment of this study was 6 participants each in the venous ulcers, bedsores, and burn wounds, while no patients with diabetic foot wounds were recruited, resulting in a total of 18 participants.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
18
HealiAid is an absorbable collagen wound dressing. It is fabricated by fibrous collagen matrix, in which the collagen is purified from bovine Achilles tendons. HealiAid can be applied easily by covering directly to the clean wound sites.
Wound Healing
The wound healing was defined as the percentage of area change at baseline and 8 weeks after treatment. The wound area was calculated by multiplying the length (direction from head to leg) by the width (widest part of the wound site, perpendicular to the length). The percentage of area change was calculated by the formula: (baseline wound area minus 8-week wound area)/baseline wound area \*100%.
Time frame: Baseline, 8 weeks after treatment
Wound Healing
The wound healing was defined as the percentage of area change at baseline and 1, 2, 4 weeks after treatment. The wound area was calculated by multiplying the length (direction from head to leg) by the width (widest part of the wound site, perpendicular to the length). The percentage of area change was calculated by the formula: (baseline wound area minus 1, 2 or 4-week wound area)/baseline wound area \*100%.
Time frame: Baseline, 1, 2, 4, 12(if needed) weeks after treatment
Duration of Wound Healing
The duration of wound healing was recorded using the subjects' diaries, which indicated the time when the wound completely healed.
Time frame: Baseline, 1, 2, 4, 12(if needed) weeks after treatment
Granulation Tissue Growth
The granulation tissue growth was defined using a scale of 6 grades. * 0: the wound site is either completely healed or shallow. * 1: the granulation tissue occupied 90% of wound area * 2: the granulation tissue occupied ≥50%, \<90% of wound area * 3: the granulation tissue occupied ≥10%, \<50% of wound area * 4: the granulation tissue occupied \<10% of wound area * 5: No granulation tissue present
Time frame: Baseline, 1, 2, 4, 8, 12(if needed) weeks after treatment
Wound Exudate
The extent of wound exudate was classified as 4 grades. * 0: No wound exudate * 1: Small amount of wound exudate, may not require daily dressing changes * 2: Moderate amount of wound exudate, requires daily dressing changes * 3: Large amount of wound exudate, dressing changes at least twice daily
Time frame: Baseline, 1, 2, 4, 8, 12(if needed) weeks after treatment
Incidence of Safety Events
The safety events were defined as the wound site infection/inflammation and scoring as: * 0: No signs of infection or inflammation. * 1: Redness, swelling, heat, and pain that indicated inflammation. * 2: Clear signs of infection such as inflammation, purulence, or odor. * 3: Systemic symptoms such as fever. Other safety events such as allergic reaction was scored as: * 0: No reaction * 1: Doubtful reaction * 2: Weak reaction * 3: Strong reaction
Time frame: week 0 to week 12
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