Evaluating the Efficacy of a Tocotrienols-Loaded Dressing in Wound Care for Pressure Ulcers
The goal of this clinical trial is to investigate the effects of the dressing containing Tocotrienols on patients with stage 1 and stage 2 pressure ulcers. The main questions it aims to answer are:
* Will the dressing containing Tocotrienols lead to a reduction in the Pressure Ulcer Scale for Healing (PUSH) Score?
* Will the dressing containing Tocotrienols help heal the participants' pressure ulcer wounds?
* Will the dressing containing Tocotrienols lead to reduction in wound surface area?
* What is the percentage of patients with completely healed wounds by the end of the study?
Researchers will compare Tocotrienols-loaded formulated dressing to conventional dressing (standard of care as control) in pressure ulcers.
Participants will:
* Have their pressure ulcers checked by a study doctor to ensure they are infection-free and suitable ulcer fitting the inclusion criteria
* Undergo 24-hour allergy testing with patch of Tocotrienol-loaded dressing and standard hydrocolloid dressing
* Be randomly assigned to one of three groups if they qualify: control, vehicle-control, or treatment group
* Assess skin sensitivity testing the next day, and if qualify, will be started on first dosing.
* Attend follow-up visits on days 1, 3, 5, 7, 15, 22, 29, 35 and 43, where additional questions and assessments will be completed.
Gender: All
Ages: 18 Years - Any
Pressure Ulcer Stage 1
Pressure Ulcers Stage II
Pressure Injuries