Rationale of Subcutaneous Levofloxacin Infiltration as an Adjunct for Surgical Site Infection Prevention in Emergency Laparotomy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSylhet M.A.G.Osmani Medical College

About this trial

Surgical site infection (SSI) remains a major cause of postoperative morbidity following emergency laparotomy, particularly in contaminated and dirty/infected abdominal conditions. Systemic antibiotic prophylaxis alone often fails to achieve adequate local tissue concentrations at the incision site due to impaired perfusion, contributing to persistently high SSI rates in this population.

This trial evaluates subcutaneous infiltration of levofloxacin, a broad-spectrum fluoroquinolone with favorable tissue penetration, administered along the wound edges immediately prior to skin closure, as an adjunct to standard surgical and antibiotic management.

This study is investigator-initiated and will be conducted as a single-center trial within the Department of Surgery, Sylhet MAG Osmani Medical College Hospital.

Eligibility criteria

Qualifiers

Patients aged 18 years and above

Patients undergoing emergency laparotomy for contaminated surgical pathology

Patients undergoing emergency laparotomy for dirty/infected surgical pathology

Disqualifiers

Patients with known hypersensitivity to levofloxacin or other fluoroquinolones

Pregnant women or lactating mothers

Patients with pre-existing severe renal impairment

Patients with pre-existing skin infection at the incision site

Trial design

Treatments tested in this trial

  • Levofloxacin

Treatment groups

90 Participants
are divided into 2 treatment groups