Assessing the Efficacy of Photodynamic Therapy for Preventing Surgical Site Infections (LIGHT)

Guy's and St Thomas' NHS Foundation Trust

Status: Enrolling

Conditions: Nasal Disease; Surgery; Light; Therapy, Complications

Treatments: Diagnostic Test: Flexible nasendoscopy; Other: In-person review; Combination Product: Photosensitizer formulation only; Other: Telephone Follow-up; Other: Standard follow-up; Diagnostic Test: Nasal culture; Device: Nasal PDT

Study type: Interventional

Funder types: Other

Identifiers

NCT06731881

IRAS345142

Details and patient eligibility

About

This is a randomised, unblinded interventional device proof of concept pilot trial in which patients undergoing nasal surgery will be selected for either photodisinfection therapy (PDT) with the Steriwave™ ND System, or control with nares swabbed with 'photosensitizer formulation' preoperatively.

This trial will primarily assess the safety and efficacy of nasal photodisinfection treatment in decreasing post-operative events in patients undergoing nasal surgery. After signing informed consent, and before surgery, participants will receive a baseline culture of the anterior nares to determine nasal bacterial colonization and will have a flexible nasendoscopy to determine their Lund-Kennedy (LK) endoscopic score. Subjects will then be randomised to nasal PDT (which includes two applications of 'photosensitizer formulation' [0.01% methylene blue with 0.25% chlorhexidine solution], two minutes apart), along with light therapy, or control with nares swabbed twice with 'photosensitizer formulation' with two minutes in between (no light therapy). Following treatment, participants will be re-cultured (2 weeks after the surgery ± 7 days) and reviewed for antibiotic use and surgical site infection (SSI) using LK endoscopic scoring. At 30 days, all participants will be followed up by telephone to review if they received antibiotics for presumed postoperative infection. Standard post-operative care will be provided according to the type of surgery performed. Any required interventions post-operatively will be documented.

Full description

Preoperative nasal decolonisation has been shown to achieve significant reductions in surgical site infections at sites remote from the nasal cavity. It would therefore seem to have great potential in reducing the risk of post-operative infections after sinonasal surgery, and therefore reduce antibiotic usage. If surgeons have confidence in the treatment, those that routinely prescribe prophylactic antibiotics may also be pursued to change their practice.

The aim of this study is to assess the efficacy and safety of photodisinfection therapy versus control with nares swabbed with 'photosensitizer formulation' (0.01% methylene blue with 0.25% chlorhexidine solution) to reduce the antibiotics usage for presumed SSI inpatients undergoing nasal surgery. The investigators hypothesise that preoperative photodisinfection will demonstrate greater efficacy compared to control with nares swabbed with 'photosensitizer formulation' (0.01% methylene blue with 0.25% chlorhexidine solution) in reducing the usage of antibiotics for presumed surgical site infection (SSI) among patients undergoing nasal surgery.

The investigators will also further evaluate the effectiveness of nasal decolonisation in eliminating colonization of the anterior nares with S. aureus and other potentially pathogenic microbes. The anterior nares are often considered the primary reservoir of S. aureus and other pathogens on the body (36). Therefore, this product could play an important role in helping to eliminate the anterior nares as a pathogen reservoir in surgical patients.

This study is meant to provide further safety, efficacy, and methodological data, but is not intended to establish definitive statistical significance. If required, this study will support a subsequent larger study that would establish statistical significance for the reduction of surgical site infections, but which is currently not the subject of this protocol.

Enrollment: 80 estimated patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients ≥ 16 years

• Patients scheduled to undergo elective:

  • Endoscopic Sinus Surgery (ESS) with or without adjunctive Septoplasty and/or Turbinoplasty
  • Septoplasty with or without adjunctive Turbinoplasty
  • Closed Septoplasty with or without adjunctive Turbinoplasty

• Judged by the Investigator as suitable for participation in the study without safety concerns based on medical history and physical examination

• Willing and able to provide written informed consent prior to participation in the clinical investigation

• Willing and able to comply with all study related procedures

Exclusion criteria

-• Patients undergoing open septorhinoplasty, anterior or septal biopsies, or post cautery

• Congenital or acquired immunodeficiency, bone marrow disease, diabetes, autoimmune conditions requiring immunosuppressive treatment, any immunosuppressive medication at the time of consent or within the last 4 weeks before randomisation
• Primary or secondary ciliary dyskinesia, cystic fibrosis
• Patients who have received antibiotics within a week before randomisation
• Patients who receive prophylactic antibiotics or antibiotics prior to discharge
• Systemic steroid treatment less than 4 weeks before randomisation
• History of frequent nose bleeds, or a condition that increases the risk of excessive bleeding
• Undergoing active cancer treatment at time of consent/ or planning to start cancer treatment within trial period or completed cancer treatment within the last 4 weeks
• Any disease, condition (medical or surgical), or drug or alcohol abuse, which, in the opinion of the investigator, might compromise the study results, or would place the patient at increased risk of infection
• Previously treated with radiation on the face, head, or neck regions
• Female patients who are pregnant or breastfeeding at the time of consent
• Received a study drug in a clinical trial for an investigational drug within the previous 30 days from consent, or 5 half-lives, whichever is longer
• Used antimicrobial wash or wipes within 7 days of randomisation or during the study period
• Patients with allergies / hypersensitivity to methylene blue, polymethyl methacrylate (PMMA), or to chlorhexidine gluconate (CHG)

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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80 participants in 2 patient groups

Photodisinfection

Active Comparator group

Description:

The photodisinfection product consists of a CE-marked light source (SW4000), a disposable single-use nasal light diffuser, and a single-use photosensitiser applicator that can be used in hospital settings.

Treatment:

Device: Nasal PDT

Diagnostic Test: Nasal culture

Other: Telephone Follow-up

Other: Standard follow-up

Other: In-person review

Diagnostic Test: Flexible nasendoscopy

Control

Active Comparator group

Description:

The control group will have nares swabbed with 'photosensitizer formulation' (0.01% methylene blue with 0.25% chlorhexidine solution) prior to surgery.

Treatment:

Diagnostic Test: Nasal culture

Other: Telephone Follow-up

Other: Standard follow-up

Combination Product: Photosensitizer formulation only

Other: In-person review

Diagnostic Test: Flexible nasendoscopy