Surgical Site Infection Clinical Trial
Official title:
Impact of Prophylactic Use of Irrisept Irrigation System for Spinal Instrumentation
Verified date | June 2024 |
Source | Lifespan |
Contact | Alexander Chernysh |
Phone | 401-444-9868 |
AChernysh[@]lifespan.org | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | May 2026 |
Est. primary completion date | May 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age: 18+ years old - Indications: deformity, oncologic, degenerative, trauma - Standard layer-by-layer closure - Locoregional flap-based closure Exclusion Criteria: - Acute/chronic open wounds (spine or non-spine) - On-going non-spinal infection within 30 days of index operation - Concurrent antibiotic use (for spine or non-spine infections) - History of prior spinal infection - Allergy to vancomycin or chlorhexidine - Suspicion for osteomyelitis - Other surgery within 90 days post-operatively fromm index - Concurrent enrollment in other trial |
Country | Name | City | State |
---|---|---|---|
United States | Rhode Island Hospital | Providence | Rhode Island |
Lead Sponsor | Collaborator |
---|---|
Jared Fridley |
United States,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Occurrence of surgical site infection | Development of infection after index spinal instrumentation | 90 days post-operatively | |
Secondary | Mortality | Capture mortality rates after index spinal instrumentation | 12 months post-operatively | |
Secondary | Duration of index hospitalization | Capture duration of index hospitalization after index spinal instrumentation | 12 months post-operatively | |
Secondary | Occurrence of 30-day readmission | Capture 30-day readmission rates after index spinal instrumentation | 30 days post-operatively | |
Secondary | Occurrence of wound dehiscence | Capture all incidences of wound dehiscence after index spinal instrumentation | 12 months post-operatively | |
Secondary | Time to closed suction drain removal | Capture the time interval to closed suction drain removal after index spinal instrumentation | 12 months post-operatively | |
Secondary | Presence of atypical micro-organisms on wound fluid laboratory culture | Capture the presence of atypical micro-organisms after index spinal instrumentation | 12 months post-operatively | |
Secondary | Cost of spine surgery care from surgery to 12-month post-operative follow up | Consider associated total costs of spinal instrumentation after index spinal instrumentation by comparing total surgical costs and post-surgical outcome expenses of those with and without Irrisept irrigation use | 12 months post-operatively |
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