Burns Clinical Trial
Official title:
Comparison of Effectiveness of Amniotic Membrane and Duoderm Dressings in Pediatric Burn Patients: a Randomized Controlled Trial
There is a difference in frequency of wound infection, mean pain score, mean of time for skin grafting and hospital stay in pediatric 2nd and 3rd degree burns, between amniotic membrane and duoderm dressings
After informed consent of the patients, patients who will fulfill the inclusion and exclusion
criteria will be enrolled in the study from Department of Pediatric Surgery, Mayo Hospital
Lahore and will be randomly allocated by lottery method into 2 groups by the doctor. Group A
and B with 86 patients in each group. Group A patients will be undergoing amniotic membrane
dressing, while group B patients will undergo colloid gel foam dressing. Basic demographic
information will be noted. Effect modifiers (hemoglobin level, weight and height) will be
noted.
In group A, the wounds will be washed with normal saline and then covered with amniotic
membrane over which a layer of Vaseline gauze will be applied and dressing with gauze and the
crape bandage will be applied. Every 3-4 days these dressings will be changed and assessed
for pain, wound infection and wound c/s will be sent. Placentas from clean vaginal deliveries
and elective C-sections will be taken. Blood of mother will be screened. Amniotic membrane
will be separated from placenta in a clean sterile bowl. Bowl will be put in refrigerator at
4 degrees.
In group B, wound will be washed with normal saline . The wound site will be covered with
Colloid Gel Foam and gauze, and crape bandage will be applied. Dressing will be changed after
3-4 days. The outcome (pain score, wound infection,time for skin grafting and hospital stay)
will be compared in both groups.
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