About this trial
randomize control trial to evaluate the efficacy of using zinc oxide versus moist exposed wound ointment in treatment of second stage pressure ulcer.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Willing to participate.
KAMC cases in medical ward, neuroscience ward, and intensive care unit.
Newly cases diagnosed with second stage pressure ulcer according to the European pressure ulcer advisory panel/national pressure ulcer advisory panel (NPUAP) guidelines.
Disqualifiers
Not consenting to participate
Patients with suspected hypersensitivity reactions to any of the topical formulation's ingredients.
Either a category III or IV pressure ulcer.
Evidence of deep tissue injury (exudative drainage, purple or maroon localized area of discolored intact skin or blood-filled blister due to pressure damage).
Trial design
Parallel
Treatments tested in this trial
MEBO Wound Ointment
Drugboth are used for second pressure ulcer
zinc oxide
Drugboth are used to treat second degree pressure ulcer but with no superiority
Treatment groups
Trial outcomes
Primary outcomes
Wound healing
Wound healing will be assessed by using Bates-Jensen Wound Assessment Tool (BWAT) daily for both treatments. (BWAT) consists of 13 items to evaluate wound size, type and depth, Each item is graded on a scale of 1 to 5, where a score of 1 indicates progress toward healing while a score of 5 indicates the absence of healing or wound deterioration. Cumulative BWAT scores vary from 13 to 65
Secondary outcomes
Recovery time
The duration of treatment will be record at the assessment sheet so Recovery time will be determined from this sheet.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.