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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03063138
Other study ID # OUH3D03
Secondary ID
Status Completed
Phase N/A
First received February 21, 2017
Last updated September 18, 2017
Start date August 1, 2015
Est. completion date March 1, 2017

Study information

Verified date September 2017
Source Odense University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to evaluate the intra- and inter-rater variability of wound measurements using the 3D camera and to compare with standard measurement methods (2D image method and gel injection). Forty-eight patients with wounds of various sizes are measured by four clinicians. Each wound is measured twice with the 3D camera, once by 2D image method and once by gel injection into wound cavity by two clinicians.


Description:

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 wound is one of the major etiologic factors for delayed healing. Wound measurement is important in monitoring the healing process of wound and in evaluating the effect of treatment. Three-dimensional methods for measuring wound size have made it possible to evaluate the process of wound healing with respect to all dimensions. The investigators have developed a 3D camera, which is able to measure wound size (2D area, 3D area, perimeter and volume) and to assess wound characteristics.

The aim of the study is to evaluate the intra- and inter-rater variability of wound measurements using the 3D camera and to compare with standard measurement methods (2D image method and gel injection). Forty-eight patients with wounds of various sizes are measured by four clinicians. Each wound is measured twice with the 3D camera, once by 2D image method and once by gel injection into wound cavity by two clinicians.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date March 1, 2017
Est. primary completion date March 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with wounds

- 18 years or older

Exclusion Criteria:

- Superficial ulcer (less than 5x5 mm with no substantial loss of subcutaneous tissue)

- Non-compliance (dementia, mental disorders)

Study Design


Locations

Country Name City State
Denmark University Centre of Wound Healing, Odense University Hospital (OUH) Odense

Sponsors (1)

Lead Sponsor Collaborator
Odense University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Wound 2D area Measured by 3D camera and 2D image method 1 day
Primary Wound 3D area Measured by 3D camera 1 day
Primary Wound perimeter Measured by 3D camera 1 day
Primary Wound volume Measured by 3D camera 1 day
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