Wound Heal Clinical Trial
Official title:
Effectiveness and Tolerability of an Overnight 4-week Treatment With Patch Containing Onion Extract and Allantoin for Cesarean Section Scars
The wound healing is a process occurring in response to dermal injury. The resulting scar may
have various characteristics ranging from fine-line and asymptomatic to hypertrophic scars
and keloids. Prevention or early treatment of pathological scars is the most appropriate
approach. Among available remedies, gels and patches containing onion extract and allantoin
have been demonstrated to be safe and effective in patients with scars of various origins and
severity.
One of the most used natural products is a patch containing allium cepa and allantoin
licensed for treatment of the scars including keloids. However, up to date, no controlled
studies have evaluated the effects of such a device in women who have undergone Cesarean
delivery. Therefore, the aim of this study was to investigate the effects of this patch on
Cesarean section (C-section) scars.
This is an observational non-interventional study. Women who underwent C-section were consecutively recruited at University Hospital of Salerno. Taking into account the number of C-section the study population was divided into two groups: Group A included subjects without a prior history of C-section, group B subjects who had already undergone previous C-section. At baseline after stitches removal, scars assessment was made using digital photographs and the validate Patient and Observer Scar Assessment Scale (POSAS). After 4 weeks, during the outpatient visit, women from both group A and B were asked whether had applied some natural products on the scars or not. In this occasion, the C-section of the women who had applied a patch containing allium cepa and allantoin as well as those of women who had not used any products (who represented the control group) were re-evaluated as at baseline. The Observers were blinded. One of them performed the scars assessment at baseline, the other one after 4 weeks. During the outpatient visit an informed consent for participation was obtained by all the subjects costituing the study population. The participation to the study was voluntary ;
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