About this trial
This randomized controlled trial aims to compare the effect of early versus delayed water exposure after cutaneous surgeries on the incidence of surgical site infections. Patients undergoing elective cutaneous surgical procedures will be randomly assigned to either early postoperative water exposure within 48 hours or delayed exposure after 7 days. Wound outcomes will be assessed using the Southampton Wound Grading System during follow-up visits. The study seeks to determine whether early water exposure is safe and whether it influences postoperative wound healing and infection rates.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients undergoing elective surgical procedures, such as excision of benign or malignant skin lesions, skin grafts, and skin biopsies.
Disqualifiers
1.Patients on anti-coagulants.
Trial design
Parallel
Treatments tested in this trial
Care as usual
BehavioralParticipants will be allowed early exposure of the postoperative wound to water following cutaneous surgery according to the study protocol.
Care as usual
BehavioralParticipants will follow conventional postoperative wound care instructions with delayed exposure of the surgical wound to water.
Treatment groups
Trial outcomes
Primary outcomes
Postoperative Surgical Site Infection
Assessment of the frequency of surgical site infection following cutaneous surgery in participants receiving early versus delayed postoperative water exposure.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: