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Clinical Trials/NCT03945357
NCT03945357
Completed
Phase 3

Reducing INfection at the Surgical SitE With Antibiotic Irrigation During Ventral Hernia Repair (RINSE Trial)

Prisma Health-Upstate1 site in 1 country250 target enrollmentMay 15, 2019

Overview

Phase
Phase 3
Intervention
Normal saline
Conditions
Ventral Hernia Repair
Sponsor
Prisma Health-Upstate
Enrollment
250
Locations
1
Primary Endpoint
Surgical Site Infection
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This is a study to determine if the incidence of infection at the Surgical SitE is impacted if with Antibiotic Irrigation is used during Ventral Hernia Repair (RINSE Trial)

Detailed Description

Surgical site infection (SSI) is common after open ventral hernia repair. Numerous factors contribute, including patient comorbidities, operative technique, and degree of contamination of the case. SSI often requires prolonged hospital length of stay (LOS), readmission, or other procedural intervention. One potential intervention to reduce SSI is the use of antibiotic irrigation, which has been shown to reduce SSI in colorectal surgery in a recent randomized control trial. We retrospectively evaluated our use of dual antibiotic irrigation at the time of mesh placement during open ventral hernia repair (OVHR), demonstrating a significant reduction in SSI (16.5 vs 5.4%) using a combination of gentamicin and clindamycin irrigation when compared to saline alone. We plan to complete a registry-based, randomized clinical trial (RCT) through the Americas Hernia Society Quality Collaborative (AHSQC) to further assess the impact of dual antibiotic irrigation on SSI after OVHR with mesh. This will include patients undergoing open retromuscular (RM) repair with or without transversus abdominis myofascial advancement flap (TAR) with placement of permanent synthetic mesh (mid-weight, large-pore polypropylene). Power analysis based on only this subset of patients from our initial study indicates a total of 210 patients are needed to demonstrate a significant reduction in SSI using antibiotic irrigation vs saline irrigation alone.

Registry
clinicaltrials.gov
Start Date
May 15, 2019
End Date
January 9, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \>18 y/o.
  • Elective, open ventral hernia repair in a retromuscular fashion, with or without TAR.
  • Clean, clean-contaminated, or contaminated wounds.

Exclusion Criteria

  • Age \<18 y/o.
  • Pregnancy.
  • Emergency hernia repair.
  • Laparoscopic, robotic, or hybrid approach.
  • Dirty wounds.
  • Use of biologic or absorbable synthetic mesh.
  • Onlay, intraperitoneal or preperitoneal mesh placement.

Arms & Interventions

Saline Irrigation

Normal saline is to be placed into the dissected retromuscular space AFTER placement and fixation of mesh. This should fill the cavity completely to the level of the skin. Irrigant is to be left to stand for a total of three minutes and then evacuated. Additional irrigation with saline PRIOR to the randomization is permitted at the surgeons' discretion for hemostasis with no requirement for duration. Additional saline irrigation of the subcutaneous space after fascia closure should be performed prior to skin closure.

Intervention: Normal saline

Antibiotic Irrigation

Antibiotic solution is prepared consisting of 240 mg gentamicin and 600 mg clindamycin in 500 ml saline to ensure proper concentration. This solution should be placed into the dissected retromuscular space AFTER placement and fixation of mesh. This should fill the cavity completely to the level of the skin. Irrigant is to be left to stand for a total of three minutes and then evacuated. Additional irrigation with saline PRIOR to the randomization is permitted at the surgeons' discretion for hemostasis with no requirement for duration. Additional antibiotic irrigation of the subcutaneous space after fascia closure should be performed prior to skin closure. This second irrigation is not timed.

Intervention: Gemcitabine/ clindamycin

Outcomes

Primary Outcomes

Surgical Site Infection

Time Frame: 30 days

Number of participants with Surgical Site Infections

Secondary Outcomes

  • Incidence of SSI Requiring Intervention(30 days)

Study Sites (1)

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