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Study identifier: NCT06439953 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Irrisept Solution for Instrumented Spine Surgery

Condition: Post-Op Complication · Spine Surgery · Site Infection  ·  Sponsor: Rhode Island Hospital

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Various spine surgeons perform wound irrigation using saline mixed with vancomycin, relying on mechanical debridement of non-viable tissue, physical disruption of biofilm, and bacteriostatic effect against gram positive flora. When used as a powder, topical application of vancomycin has demonstrated increased risk of symptomatic seroma formation, which is an adverse outcome that often requires bedside or intra-operative aspiration. Broad-spectrum antiseptic agents, such as Irrisept, offer bacteriocidal properties to eliminate hardware inoculation, thereby minimizing the risk of deep space infection, while obviating the risk of seroma development.

This description comes directly from the study's public registry record.

Talk to the study team

Alexander Chernysh  ·  401-444-9868  ·  AChernysh@lifespan.org

Owen Leary  ·  401-6068388  ·  owen.leary@lifespan.org

Always discuss trial participation with your own doctor first.

Locations (1)

Rhode Island HospitalProvidence, Rhode Island, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06439953