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Completed

NCT Number: NCT02315092

Evaluation of Fluorescence-image Guided Wound Assessment vs. Standard Practice

The current trial aims to compare the assessment of diabetic foot ulcers by fluorescence image guidance to standard practice. The device will be used to acquire fluorescence images of diabetic foot ulcers: when wounds are illuminated by violet/blue light, most pathogenic bacterial species emit a unique red fluorescence signal. The device is intended to be used as part of the clinical assessment process, which may include visual assessment, signs of heat or high temperature, the presence of exudate, and redness in the area. Images will guide the clinician to inspect, sample or further evaluate areas where fluorescing bacteria is present. This study will allow us to determine the benefit of fluorescence image-guided procedure as compared to standard clinical practice to assess bacterial burden in diabetic foot ulcers. Microbiological swabbing under standard practice and fluoresce-guided imaging will be performed in order to compare the two techniques.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Judy Dan Research and Treatment Centre

Toronto, Ontario, M2R1N5, Canada

About this study

Chronic wounds and their associated care are a burden to patients and health care systems worldwide. Microbiological testing of wound samples is often used to identify and quantify bacterial species, the latter of which may be both an objective quantitative indicator of infection and a predictive correlate of healing. Microbiology reports contain useful information about microbial identities, antibiotic susceptibility, and semi-quantitative bacterial growth rates, but these data typically represent the bacterial load in the wound centre only, and often arrive 3-5 days later. There is an unmet clinical need to improve the microbiological sampling and treatment of wound infections. To address this need, we developed a handheld portable imaging device that obtains white light (WL) and fluorescence (FL) images (or video) of normal skin and wounds in high-resolution and in real-time, which can be used at the point-of-care. It was demonstrated in previous studies that the device1) provides image-guidance for tissue sampling, detecting clinically-significant levels of pathogenic bacteria and wound infection otherwise overlooked by conventional sampling and 2) provides image-guidance for wound treatment, accelerating wound closure compared with conventional therapies and quantitatively tracking long-term changes in bacterial bioburden and distribution in wounds.

The current trial aims to compare the assessment of diabetic foot ulcers by fluorescence image guidance to standard practice. The device will be used to acquire fluorescence images of diabetic foot ulcers: when wounds are illuminated by violet/blue light, most pathogenic bacterial species emit a unique red fluorescence signal. The device is intended to be used as part of the clinical assessment process, which may include visual assessment, signs of heat or high temperature, the presence of exudate, and redness in the area. Images will guide the clinician to inspect, sample or further evaluate areas where fluorescing bacteria is present. This study will allow us to determine the benefit of fluorescence image-guided procedure as compared to standard clinical practice to assess bacterial burden in diabetic foot ulcers. Microbiological swabbing under standard practice and fluoresce-guided imaging will be performed in order to compare the two techniques.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female who present with a diabetic foot ulcer and are receiving standard wound care treatment.
  • 18 years and older

Exclusion criteria

  • Treatment with an investigational drug within 1 month before study enrolment
  • Inability to consent
  • Any contra-indication to routine wound care and/or monitoring

Treatment and study plan

Fluorescence Imaging

Device

Wounds will be imaged using violet light (405 nm) illumination to locate areas with bacterial presence to guide swabbing.

Primary outcomes

  1. Correlation of localized fluorescence signals in acquired images with microbiological samples

    Time frame: At study visit (only one study visit)

    Microbiological swabs will be taking from fluorescence positive regions to correlate with bacterial presence

  2. Comparison of number/variety of bacteria obtained by fluorescence-guided sampling vs. standard practice

    Time frame: At study visit (only one study visit)

    Microbiological swabs will be taking from the wound using standard practice and following fluorescence-image guidance

Secondary outcomes

  1. Assessment of the clinical functionality of the K2 Imaging Device

    Time frame: At study visit (only one study visit)

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Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Judy Dan Research and Treatment Centre

Registry information

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Dec 11, 2014
Registry last updated
Feb 13, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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