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Clinical Validation of a 'Hand-held' Fluorescence Digital Imaging Device for Wound Care Applications

NCT01378728 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2017-05-19

No results posted yet for this study

Summary

The primary objective of this clinical study is to evaluate the use and effectiveness of our 'handheld' fluorescence digital imaging device platform for real-time non-invasive clinical monitoring of chronic wounds for healing and bacterial contamination/infectious status over time. This will enable us to determine if the device can detect and longitudinally track intrinsic changes that may occur during the wound healing process including, but not limited to, collagen re-modeling and bacterial infection of the wound site.

Conditions

  • Wounds

Sponsors & Collaborators

  • University Health Network, Toronto

    lead OTHER

Principal Investigators

  • Ralph S DaCosta, PhD · Ontario Cancer Institute, University Health Network

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2017-04-30
Completion
2017-04-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01378728 on ClinicalTrials.gov