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Effect of Autologous Fat Grafting on Acute Burn Wound Healing

Phase 3
Completed
Conditions
Burns
Interventions
Drug: Topical Cream
Procedure: autologous fat grafting
Procedure: split thickness skin grafting
Registration Number
NCT03791710
Lead Sponsor
Ahmed Mohamed Abouzaid
Brief Summary

the study evaluates the role of autologous fat grafting and the usage of nanofat in the treatment of the acute burn injuries in different genders and its influences on the healing time and hospital stay, pain control, the need and take of a split thickness skin graft and its size, and the end resulting early scarring, in comparison with control group that were treated with traditional methods, so as to find out new method of treating burn injuries and decreasing its morbidity.

Detailed Description

as the patient is admitted, full evaluation locally ( as regard the wound itself and the areas of fat harvesting) and generally (assessment of the general condition) is done, fluid resuscitation is started as the unit protocol hand in hand with the analgesia and other medications prescribed according to the unit protocol.

the patient's general condition is optimized for surgery of the fat extraction and grafting which typically should be within the first 6 days of admission.

then under anesthesia (any possible type from local and regional up to general anesthesia) liposuction procedure is performed, then fat is processed then grafted at the wound site with other portion prepared as nanofat for topical use and wound coverage, then sterile dressing is applied.

typically follow up is held daily with the dressing change day after another with the use of the nanofat only and sterile dressing

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • both males and females within the age frame are candidates.
  • previously healthy individuals with no co-morbid conditions e.g cardiac, hepatic, diabetic, vascular or renal disease.
  • with TBSA of 10 to 30% affected and of deep dermal to full thickness wound depth, at any part of the body except the genitalia, perineum or the perianal region or those with inhalational injury.
Exclusion Criteria
  • other patients aged younger or older than the specified age group.
  • patients with co-morbid conditions.
  • patients with smaller or larger BSA than the specified BSA.
  • burns involving the genitalia, perineum or the perianal region and patients with inhalational injury.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control groupsplit thickness skin graftingthis group of patients are treated with the regular conventional methods like application of topical agents e.g silver sulphadiazine
control groupTopical Creamthis group of patients are treated with the regular conventional methods like application of topical agents e.g silver sulphadiazine
fat grafting groupsplit thickness skin graftingthis group of patients will have the autologous fat grafting for their burn wounds
fat grafting groupautologous fat graftingthis group of patients will have the autologous fat grafting for their burn wounds
Primary Outcome Measures
NameTimeMethod
wound healing timeone to three weeks

the effect of the fat grafting on the wound healing time

Secondary Outcome Measures
NameTimeMethod
effect on pain perception, subjective assessment scaleimmediate post-operative and up to three weeks

effect of the fat grafting on the pain sensation in the burn wound, assessment through a numerical scale starting at "0" indicating no pain at all to "10" the most intense severe pain. the range between "1" and "3" describes mild pain, between "4" and "6" describes moderate pain, and lastly from "7" to "10" severe pain.

Trial Locations

Locations (1)

Abouqir General Hospital

🇪🇬

Alexandria, Egypt

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