Postoperative Ozonated Oil Dressing After Open Inguinal Hernia Repair: A Randomized Pilot Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorNigde Omer Halisdemir University

About this trial

This study looks at whether a special wound dressing containing ozonated oil can reduce early wound inflammation after open inguinal hernia surgery. Open inguinal hernia repair is a common operation, and although infection rates are low, many patients experience redness, swelling, tenderness, or discomfort at the surgical site during the first days after surgery.

Participants undergoing elective open inguinal hernia repair will be randomly assigned to receive either an ozonated oil-impregnated dressing or a standard sterile dressing after the operation. The main outcome is the level of wound inflammation measured on the third day after surgery. Other outcomes include wound temperature, pain levels, cosmetic healing, and wound-related problems during the first 30 days.

The ozonated oil used in this study is a CE-certified medical product that is already used in routine wound care. This pilot study aims to provide preliminary data to help determine whether ozonated oil dressing may improve early wound healing compared with standard care.

Eligibility criteria

Qualifiers

Adults aged 18 to 75 years

ASA physical status I-III

Scheduled for elective, unilateral open inguinal hernia repair

Able to provide written informed consent

Disqualifiers

Emergency inguinal hernia (incarcerated or strangulated)

Recurrent inguinal hernia

Concomitant surgical procedures during the same operation

Immunosuppression or long-term systemic steroid use

Trial design

Treatments tested in this trial

  • ozonated oil
  • Standard Sterile Dressing

Treatment groups

60 Participants
are divided into 2 treatment groups