IRCT20210918052511N2
Recruiting
Phase 2
Assessment of the efficacy of hydrogel-based wound dressing containing allantoin and silver nanoparticles in the treatment of second-degree burn wounds: A randomized clinical trial
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Burn patients.
- Sponsor
- Mashhad University of Medical Sciences
- Enrollment
- 86
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients between the ages of 2 and 60 are eligible to participate.
- •Patients with second\-degree burns diagnosed by the relevant physician
- •Patients with burns that are less than or equal to 20%
- •Patient with second\-degree burns in upper and lower limbs and anterior trunk
- •The wound is examined by a plastic and burn surgeon for necrosis and the depth of the burn. If the burned area is not a candidate for early surgery and can be healed without surgery and with minimal complications, the patient will be eligible to the study.
Exclusion Criteria
- •Delayed visit and the presence of obvious wound infection at the first visit by an infectious disease specialist
- •Patients who are receiving chemotherapy
- •Patients taking corticosteroids or cytotoxic medicines
- •Cancer, cytotoxic drugs, immunosuppressants, and the presence of chronic diseases other than diabetes that affect wound healing, such as severe vascular disease, lupus, rheumatoid arthritis, and renal failure
- •The presence of an underlying disease leads to a defective immune system
- •Diabetic patients
- •Taking drugs that lead to a defective immune system.
- •Burns in the back of the trunk, face, head and perineum
Outcomes
Primary Outcomes
Not specified
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