Effect of Mebo Dressing Versus Standard Care on Managing Donor and Recipient Sites of Split-thickness Skin Graft (EMD-SCZ-SGS)

Zagazig University

Status and phase: Unknown; Phase 1

Conditions: Burns

Treatments: Drug: Zagazig; Drug: Moist Exposed Burn Ointment (MEBO)

Study type: Interventional

Funder types: Other

Identifiers

NCT02737943

2579

Details and patient eligibility

About

40 Egyptian Cases with split-thickness skin graft receiving treatment at Zagazig University Hospitals. Study Duration:6 Months .Description of Agent or Moist Exposed Burn Ointment (MEBO).

Intervention:

Objectives: Primary: to determine the efficacy of MEBO versus standard care in improving the healing speed and re-epithelization process of skin graft donor and recipient sites. Secondary to determine the efficacy of MEBO in decreasing recovery time, rate of infections, rate of complications, total treatment costs and its effect on improving pain alleviation.

Description of Study Design: Arm 1 20 MEBO at sites of donor graft and recipient at time of operation and in dressing Arm 2 20 Standard cream Zagazig University Hospital (Antibiotics & analgesics) Estimated Time to Complete 5 months

Full description

Background Information.

Skin grafting is a frequently used technique for covering skin defects in cases of row area. The technique evolved from use in the back alleys of India in pre-Christian times to become one of the most valuable clinical tools in modern surgery. There are several techniques for caring for the skin graft site to assure an adequate graft and prompt as well as wound healing.

The use of the split-thickness skin graft (STSG) as reconstructive technique is very common nowadays but this technique is usually a source of pain and discomfort for the patients and may cause significant morbidity and result in hypertrophic or even keloid scarring. The wound heals by a process of re-epithelialization which results in an epithelial cover usually within 7-14 days. The aim of graft management is to maintain an environment that promotes optimal healing and prevents morbidity, which can include pain and infection and ultimately delayed healing.

The dressing of donor and recipient sites which provides a protective barrier should be easy to apply, promote rapid re-epithelialization, and be pain free, infection free, and relatively inexpensive.

MEBO have been proved to have anti-inflammatory and anti-microbial effect due to the presence of - β sitosterol and berberine respectively. Many studies have reported that MEBO provides suitable moist environment needed for burn wounds for optimal healing and re-epithelialization without the need for wound closure by dressing. Also some studies have proved the efficacy of MEBO in secondary healing of partial thickness wounds, such as split thickness skin graft sites, with improved cosmetic results and better scar quality.

In cases of raw area, donor and recipient sites have been traditionally dressed with low-adherent wound contact paraffin gauze or antibiotic-impregnated tulle gras and covered by a secondary dressing made of gauze and absorbent padding.

These dressings are relatively inexpensive. However, during the peri-operative period, patients complain more often of discomfort or pain at the donor area than at the graft site itself besides, the poor cosmetic appearance of donor sites after healing is not readily accepted.

Because the basic pathology of burns closely mimics many aspects of skin graft donor sites, researchers are investigating using MEBO at donor and recipient sites.

Potential Risks

Due its pure and natural origin, MEBO have been reported to have no side effect or potential risks except rare cases of allergy and hypersensitivity.

Known Potential Benefits

MEBO has been proved to have a positive effect on improving healing process with rapid re-epithelialization. According to a recent study, the burn areas and graft sites were markedly less hyperemic and less pigmented and the final cosmetic appearance and patient satisfaction were also higher by using MEBO. The cases who used MEBO had better scar assessment and lower pain scale.

Enrollment: 40 estimated patients

Sex: All

Ages: 2 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patients who will be managed using split-thickness skin graft.
2. Donor skin grafts are harvested from a site in the thigh (a minimum of 5 x 5-cm total area).
3. Intention for treatment at Zagazig University.
4. Age between 2 & 60 years.
5. An approved informed consent and authorization permitting release of personal health information must be signed by patient or guardian.
6. Compliance with treatment for 3 weeks.
7. Patients of childbearing age must have a negative pregnancy test.

Exclusion criteria

1. Chemical or electrical burns.
2. Patient with concomitant injury of head trauma, inhalation injury, or bone fracture.
3. Pregnant or breast-feeding female.
4. Known or suspected allergies to any of the components of MEBO.
5. Suspicion or presence of active systemic or local cancer or tumor of any kind.
6. Any immune deficiency disorder.
7. Suspected alcohol or drug abuse.
8. Participation in another investigational drug study within 30 days prior to treatment start.
9. If the donor site is less than 5 x 5-cm total area.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

40 participants in 2 patient groups, including a placebo group

Arm1 Mebo

Experimental group

Description:

20 : receiving Moist Exposed Burn Ointment (MEBO) at sites of donor graft and recipient at time of operation and in dressing

Treatment:

Drug: Moist Exposed Burn Ointment (MEBO)

Arm2 Placebo

Placebo Comparator group

Description:

20 : receiving Standard cream Zagazig University Hospital (Antibiotics \& analgesics)

Treatment:

Drug: Zagazig