Suprafascial Vancomycin Powder for Prevention of Surgical Site Infections After Instrumented Posterior Spinal Fusion

Surgical Site Infection Clinical Trial

— VANCO  

Official title:

Suprafascial Vancomycin Powder for Prevention of Surgical Site Infections After Instrumented Posterior Spinal Fusion

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04017468
• Other study ID #: 2019-01143
• Status: Recruiting
• Phase: Phase 2
• Start date: October 15, 2019
• Est. completion date: March 31, 2027

Study information

• Verified date: April 2024
• Source: Insel Gruppe AG, University Hospital Bern
• Contact: Ralph Schaer, MD
• Phone: +41316322409
• Email: ralph.schaer[@]insel.ch
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Surgical site infections (SSI) after spine surgery may occur in up to 12% of cases and can lead to increased morbidity, and healthcare costs In this randomized controlled trial the investigators aim to prospectively investigate the efficacy and safety of suprafascial intrawound vancomycin powder in reducing the rate of SSIs after instrumented spinal fusion surgery. Secondary aims of the study are the incidence of vancomycin-related complications, vancomycin-resistant bacterial infections in the treatment arm as well as the rate of revision surgeries due to SSIs.

Description:

Background: Surgical site infections (SSI) after spine surgery may occur in up to 12% of cases and can lead to increased morbidity, and healthcare costs. Numerous retrospective studies suggest the use of intrawound (subfascial) vancomycin powder in spine surgery to be protective against SSIs. Adverse events, such as seroma formation or neurotoxicity may be associated with the subfascial use of vancomycin powder in high doses in direct proximity to exposed neural structures. Only one retrospective study investigated the use of suprafascial vancomycin powder. The use of intrawound vancomycin powder is controversial and there is a paucity of well-designed prospective trials evaluating its efficacy and safety in spine surgery. Objective: The main objective of this Trial is to evaluate the efficacy and safety of suprafascially applied vancomycin powder in open instrumented spine surgery to prevent surgical site infections and inform a future phase-III trial. Methods: In addition to standard preoperative systemic antibiotic prophylaxis (SAP), patients in the treatment arm will receive 1-2 g of vancomycin powder (VP) applied above the closed muscle fascia (suprafascial) into the wound at conclusion of the surgery. Patients in the control arm will not receive additional intrawound vancomycin powder. All other intra- and perioperative procedures will be conducted according to standard of practice (SOP) at the respective Trial site. All patient follow-ups and assessment of the surgical site will be observational in nature and adhere to Standard Operating Procedure (SOP) of the Trial site. All patients will be followed up clinically with conventional radiographs after 6 weeks and 3 months after surgery. At each follow-up, clinical assessment and inspection of the surgical site (the wound) will be performed by a blinded assessor (who was not present at index surgery). In cases of evident or suspected SSI standard blood samples and - if required to rule out or confirm a deep SSI - a MRI will be ordered.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 450
• Est. completion date: March 31, 2027
• Est. primary completion date: September 30, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients = 18 years of age requiring open instrumented dorsal spinal fusion of at least 1 level (involving two adjacent vertebras and one intervertebral disc)
• Signed informed consent

Exclusion Criteria:

• Preoperative ongoing infectious disease present as judged by primary surgeon (based on lab results and clinical assessment);
• Previous spine surgery at index level within last 90 days;
• Known allergy to vancomycin;
• Percutaneous or transmuscular instrumentation (minimally-invasive surgery) only without lumbar interbody fusion;
• Postoperative radiotherapy of surgical site required (e.g. for tumor)
• Preexisting cochlea damage OR known history of hearing loss NOT clearly associated with age-related hearing impairment (presbycusis);
• Renal insufficiency with stage 4 chronic kidney disease (CKD) with a glomerular filtration rate (GFR) of 15-30 ml/min or worse;
• Pregnancy or breastfeeding women;
• Participation in other ongoing clinical trials;
• Patients lacking capacity to consent;

Related Conditions & MeSH terms

• Communicable Diseases
• Infections
• Surgical Site Infection
• Surgical Wound Infection

Intervention

Drug:
• Vancomycin
Patients randomized into the treatment arm will receive 1-2 g of vancomycin powder (Vancocin® i.v.) which will be administered above the closed muscle fascia (suprafascially) before closing the subcutaneous tissue and skin. The dose of the drug will depend on the length of the skin incision: 1 g for incisions = 20 cm, 2 g for incisions = 20 cm.

Locations

Country	Name	City	State
Switzerland	Lindenhofspital Bern	Bern
Switzerland	University Hostpital Bern, Department of Neurosurgery	Bern
Switzerland	University Hostpital Bern, Department of orthopaedy	Bern
Switzerland	Spitalzentrum Biel	Biel
Switzerland	Klinik St. Anna	Luzern
Switzerland	Kantonsspital St. Gallen	St. Gallen	Saint Gallen
Switzerland	Schulthess Klinik	Zürich
Switzerland	University Hospital Zurich, Department of Neurosurgery	Zürich

Sponsors (2)

Lead Sponsor	Collaborator
Insel Gruppe AG, University Hospital Bern	University Hospital Freiburg

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of superficial and deep SSIs (according to CDC criteria)		within 90 days following index surgery
Secondary	Rate of revision surgery due to SSIs		within 90 days following index surgery
Secondary	Rate of vancomycin-resistant bacterial infections in the treatment group		within 90 days following index surgery
Secondary	Rate of vancomycin-related adverse events both locally and systemically		within 90 days following index surgery
Secondary	Rate of wound healing disorders without SSI within		within 90 days following index surgery
Secondary	Rate of wound seromas		within 90 days following index surgery
Secondary	numeric rating scale (NRS) to assess pain intensity self-reported by the patient (Score 0-10 with 0 representing no pain, and 10 maximum pain intensity) at Visits 3, 4, 5 and 6 for neck or back pain depending on surgical level (cervical or lumbosacral)		day 4, day 5, day 42, day 90
Secondary	numeric rating scale (NRS) to assess pain intensity self-reported by the patient (Score 0-10 with 0 representing no pain, and 10 maximum pain intensity) at Visits 3, 4, 5 and 6 for leg or arm pain (cervical or lumbosacral)		day 4, day 5, day 42, day 90
Secondary	Quality of life (EuroQoL 5D-5L), Mobility, Self-Care, Usual Activities, Pain/Discomfort, Anxiety/ Depression (rating from no problems to extreme problems) and health status self rating by patient (Score 0-100, 0 the worst health and 100 the best health)		day 42 and day 90
Secondary	Length of hospital stay		within 90 days following index surgery
Secondary	Cost of treatment for cost analysis between both treatment arms		1 year after index surgery
Secondary	Rate of bony fusion at the level of index surgery as assessed by CT		1 year after index surgery