MedPath

CO2-Laser Treatment in Patients With Diabetic Infected Foot Ulcers

Not Applicable
Completed
Conditions
Diabetic Foot Ulcer
Interventions
Procedure: traditional surgery
Procedure: CO2 laser
Registration Number
NCT02677779
Lead Sponsor
Azienda Ospedaliero-Universitaria Careggi
Brief Summary

The study is aimed at comparing debridement either with CO2 laser or traditional surgery in patients with infected diabetic foot ulcers. The principal endpoint is bacterial load immediately after treatment.

Detailed Description

The present study is designed to assess the antimicrobial effect of a single CO2 laser beam (DEKA SmartXide2 c80-El.En, Florence Italy) in the treatment of diabetic infected foot ulcers. CO2 laser debridement will be compared with standard surgical care. The primary efficacy endpoint will be the reduction of bacterial load between pre- and immediately after debridement. Secondary endpoints will be adverse events and pain during treatment. Two bacterial sample with a flocked nylon swab will be collected before and after debridement.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Diabetes
  • Infected foot ulcer (with clinical signs of infection)
  • Ulcer area between 0.5 and 150 cm2
  • More than 50% of ulcer area covered by fibrin and/or necrosis
  • Texas score <3
Exclusion Criteria
  • Need for revascularization
  • Pregnancy or lactation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Traditional surgerytraditional surgeryUlcer debridement with traditional surgery
CO2 laserCO2 laserUlcer debridement with laser-CO2 (DEKA SmartXide2 c80-El.En, Florence Italy)
Primary Outcome Measures
NameTimeMethod
Bacterial LoadPercent change in bacterial colonies from baseline. Variation from baseline and immediately after the end of procedure.

Percent change in bacterial colonies from baseline.

Secondary Outcome Measures
NameTimeMethod
Bleeding: Proportion of Patients With Bleeding Necessitating Haemostasisduring procedure

proportion of patients with bleeding necessitating haemostasis

Fibrin: Percent of Ulcer Area Covered by FibrinBaseline and immediately after the end of procedure

Percent change of ulcer area covered by fibrin from baseline to immediately after the end of procedure

Pain: Scores of Brief Pain InventoryDuring procedure.

Scores of Brief Pain Inventory. Scale ranges: from 0 to 10. 0 = No pain; 10= Pain as bad as you can imagine.

Granulation: Percent of Ulcer Area Covered by Granulation.Baseline and immediately after procedure

Percent change of ulcer area covered by granulation from baseline to immediately after the end of procedure.

© Copyright 2025. All Rights Reserved by MedPath