Pilot Study Comparing Taliderm™ Dressing Versus Standard of Care for Open Incision and Drainage of Wounds
Status
Completed
Conditions
Wounds
Treatments
Other: standard wet to dry dressing with gauze
Other: Taliderm™
Details and patient eligibility
About
To evaluate wound healing with the use of Taliderm™ dressing and compare it to wet to dry dressing in the treatment of open wounds after incision and drainage.
Enrollment
56 patients
Sex
All
Ages
18+ years old
Volunteers
No Healthy Volunteers
Inclusion criteria
- Inpatients with soft tissue abscess that will result in an open surgical wounds greater than or equal to 4 cms in any dimension
- Wound will require serial dressing changes
- Greater than or equal to 18 years of age
- Ability to obtain informed consent
Exclusion criteria
- Inability to obtain informed consent
- Pregnancy
- Prisoner
Trial design
Primary purpose
Treatment
Allocation
Randomized
Interventional model
Parallel Assignment
Masking
Single Blind
56 participants in 3 patient groups
Group II
Active Comparator group
Description:
Taliderm™ dressing applied until the next scheduled dressing change (up to eight hours), then replaced by a gauze dressing. Gauze dressing changes will continue per standard of care until the scheduled follow-up visits (first or second visit). At the scheduled follow-up visits, the subject will have a Taliderm™ dressing applied and left in place until the next scheduled dressing change (up to eight hours), then will continue standard of care wet to dry gauze dressing changes until next scheduled follow-up visit.
Treatment:
Other: Taliderm™
Other: Taliderm™
III
Other group
Description:
standard wet to dry dressing with gauze
Treatment:
Other: standard wet to dry dressing with gauze
group I
Active Comparator group
Description:
Taliderm™ dressing applied until the next scheduled dressing change (up to eight hours), then replaced by a gauze dressing
Treatment:
Other: Taliderm™
Other: Taliderm™
Trial contacts and locations
1
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Data sourced from clinicaltrials.gov
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