The Effect of Intraoperative Peritoneal Lavage With Super-Oxidized Solution on Surgical Site Infections and Mortality in Patients With Secondary Peritonitis: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Secondary peritonitis is a frequent abdominal emergency that is still associated with a high morbidity and mortality rate due to surgical site infections (SSI) and sepsis. Early surgical source control is crucial to avoid sepsis and worse outcomes. The current randomized controlled trial aims to investigate the effect of peritoneal lavage with super-oxidized solution (SOS) on SSI and mortality in patients undergoing emergency abdominal surgery for secondary peritonitis. The investigators hypothesize that peritoneal lavage with SOS reduces the incidence of SSI and mortality in this patient population.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Secondary peritonitis due to suspected hollow viscus perforation, anastomotic insufficiency, and/or abdominal abscess (including patients with the named abdominal emergencies as a complication after elective surgery)

• Scheduled emergency abdominal surgery by laparotomy with peritoneal lavage

• Age over 18 years

• Written informed consent

Locations
Other Locations
Switzerland
Inselspital, Bern University Hospital
RECRUITING
Bern
Contact Information
Primary
Tobias Haltmeier, MD
tobias.haltmeier@insel.ch
+41 31 664 03 04
Time Frame
Start Date: 2023-03-21
Estimated Completion Date: 2025-04
Participants
Target number of participants: 200
Treatments
Experimental: SOS group
Peritoneal lavage with super-oxidized solution (SOS)
Active_comparator: Control group
Peritoneal lavage with Ringer's solution
Sponsors
Leads: Insel Gruppe AG, University Hospital Bern

This content was sourced from clinicaltrials.gov