Three-dimensional Measurements of Diabetic Foot Ulcers

March 11, 2019 updated by: Line Bisgaard Jørgensen, Odense University Hospital

Three-dimensional Measurements for Monitoring Wound Healing of Diabetic Foot Ulcers

Diabetic foot ulcers constitute an increasing health problem in Denmark concurrent with an ageing population and an increase in diabetes prevalence. Diabetic foot ulcers belong to the most serious and costly complications. Several studies have found that the size and depth of the ulcer is one of the major etiologic factors for delayed healing. Wound measurement is important in the monitoring of the wound healing process. For the last decade different 3D (three-dimensional) techniques for measuring wounds have been proposed in order to measure wound volume, but none of the technologies have been widely used. A 3D Wound Assessment Monitor (WAM) camera has been developed, which is able to measure wound size in 3D and to assess wound characteristics.

The investigators hypothesize that three-dimensional measurements of diabetic foot ulcers are feasible in the assessment of wound healing. A prospective cohort study is conducted in which newly admitted patients with a diabetic foot ulcer are included at the first visit at the multidisciplinary clinic. The patients are followed for one year or until complete wound healing, amputation or death. The four wound measurements: 2D area, 3D area, perimeter and volume are measured using the 3D-WAM camera with frequent intervals. Patient anthropometrics and wound data are collected during the study and correlated to the wound healing.

Study Overview

Detailed Description

Method

Newly admitted patients with a diabetic foot ulcer are included at the first visit in the multidisciplinary clinic. The data mentioned below are collected at the first visit and the following examinations are performed including 3D photos. The wound size (2D area, 3D area, perimeter and volume) are estimated from the photos using the 3D-WAM camera. The wound examination is repeated after 2, 4, 8, 12, 24, 36 and 52 weeks or until healing of the wound. The wound healing is estimated using changes in wound size per time unit. Patients are treated by standard ulcer treatment methods and are unaffected by the project per se. During the trial the different methods of treatment are noted including changes from initial treatment. The variables will be quantified after one year depending on time to heal, establishment of a chronic ulcer (non-healing after one year) or an amputation has been performed.

At baseline the following patient data will be collected:

  • Demographic data: gender, age
  • Smoking habits
  • Time period between onset of wound to first visit in the multidisciplinary clinic
  • Body Mass Index
  • Comorbidity using Charlson Comorbidity Index score
  • Type of diabetes, duration of diabetes
  • Diabetic complications including retinopathy, albuminuria, coronary heart diseases and neuropathy

The following examinations will be performed at baseline:

  • Blood pressure measurement
  • Peripheral blood pressure
  • Examination for neuropathy using monofilament
  • Blood samples from patients with a diabetic foot ulcer

The clinical examination of the ulcer are performed at baseline and after 2, 4, 8, 12, 24, 36 and 52 weeks or until wound healing:

  • Size of wound (2D area, 3D area, perimeter, volume) measured using the 3D-WAM camera
  • Size of wound in 2D area using the digital imaging method with the software ImageJ
  • Location of the ulcer
  • Classification of ulcer: granulation, necrosis, epithelialisation
  • Secretory potential
  • Foot deformity
  • Bone affection - if osteitis is suspected an x-ray is taken
  • Signs of infection

The different types of ulcer treatment is registered for every ulcer:

  • Type of bandage
  • Antibiotics (local, systemic)
  • Revision (method, frequency),
  • Surgery

Effect variables

  • Wound 2D area, 3D area, perimeter and volume
  • Variation in 2D and 3D area measurements during the study period
  • Percentage change in wound size after 2, 4, 8, 12, 24, 36 and 52 weeks

Endpoints

  • Wound healing
  • Amputations
  • Chronic wound (non-healing after 1 year)
  • Death

Significance

This project seeks to clarify whether 3D photos of wounds will provide accurate structural measures to illuminate the background for delayed ulcer healing, and thereby to create platform for a more evidence based treatment algorithm.

Study Type

Observational

Enrollment (Actual)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Odense, Denmark, 5000
        • University Centre of Wound Healing, Odense University Hospital (OUH)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Newly admitted patients with diabetic foot ulcer to University Centre for Wound Healing, Odense University Hospital.

Description

Inclusion Criteria:

  • Newly admitted patients with diabetic foot ulcers
  • 18 years or older

Exclusion Criteria:

  • Superficial wound (less than 5x5 mm with no substantial loss of subcutaneous tissue)
  • Non-compliance (dementia, mental disorders)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Diabetic foot ulcers
Newly referred patients with diabetic foot ulcers from the multidisciplinary clinic: University Centre for Wound healing, Odense University Hospital, Denmark.
Three-dimensional wound measurement (2D area, 3D area, perimeter, volume) using 3D-WAM camera
Other Names:
  • 3D-WAM camera

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Wound healing change quantified using the 3D-WAM camera
Time Frame: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
The 3D wound measurements at week 2, 4, 8, 12, 24, 36 and 52 are compared to the baseline measurement at week 0.
Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
Wound healing change quantified using digital imaging method
Time Frame: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
The 2D wound measurements at week 2, 4, 8, 12, 24, 36 and 52 are compared to the baseline measurement at week 0.
Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The variability in 2D area and 3D area measurements
Time Frame: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
The variability in 2D area (digital imaging method) and 3D area wound measurements (3D-WAM camera) at week 0, 2, 4, 8, 12, 24, 36 and 52 are compared
Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
Diabetes type is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
Type 1 and 2
Baseline until healing, amputation or chronic wound (52 weeks)
Diabetes duration is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
In years
Baseline until healing, amputation or chronic wound (52 weeks)
BMI (kg/m2) is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
kg/m2
Baseline until healing, amputation or chronic wound (52 weeks)
Charlson index score is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
In groups
Baseline until healing, amputation or chronic wound (52 weeks)
HbA1c is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
mmol/mol
Baseline until healing, amputation or chronic wound (52 weeks)
Ischemia is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
Ischemia is defined by ankle pressure below 70 mmHg and/or toe pressure below 45 mmHg
Baseline until healing, amputation or chronic wound (52 weeks)
Neuropathy is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
Neuropathy is measured by Semmes Weinstein monofilament examination
Baseline until healing, amputation or chronic wound (52 weeks)
Wound duration is compared to outcome of the wound
Time Frame: Baseline until healing, amputation or chronic wound (52 weeks)
In weeks
Baseline until healing, amputation or chronic wound (52 weeks)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of life (Questionaires) using 36-Item Short Form Survey (SF-36) is compared to outcome of the wound
Time Frame: Baseline, 24 and 52 weeks
The higher the score the less disability
Baseline, 24 and 52 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Knud Yderstræde, MD, PhD, Department of Endocrinology, Odense University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2015

Primary Completion (Actual)

December 1, 2018

Study Completion (Actual)

December 1, 2018

Study Registration Dates

First Submitted

April 15, 2015

First Submitted That Met QC Criteria

April 19, 2015

First Posted (Estimate)

April 22, 2015

Study Record Updates

Last Update Posted (Actual)

March 13, 2019

Last Update Submitted That Met QC Criteria

March 11, 2019

Last Verified

March 1, 2019

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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