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MolecuLightDX Measurement Feature Clinical Validation

Wounds | Wound of Skin

This is a prospective, single-arm, paired clinical evaluation of the MolecuLightDX device in the measurement of surface wounds in patients.

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Participation Requirements

  • Sex:

    ALL

  • Eligible Ages:

    22 and up

Participation Criteria

Inclusion Criteria:

* Willing to consent
* Willing to comply with all study procedures and availability for the duration of the study
* Male or female, aged over 22 years old
* Presented with diabetic foot ulcers, venous, arterial and pressure ulcers
* Wound size is greater than 0.5 cm2
* The wound has well-defined wound borders

Exclusion Criteria:

* Circumferential wound
* Wound without clearly defined wound borders
* Wound located in a difficult to reach/measure location
* Any contra-indication to routine wound care and/or monitoring
* Wounds with a length greater than 18.5cm or a width greater than 13.5cm.
* Tunneled or undermined wounds

Study Location

SHN Research Institute
SHN Research Institute
Scarborough, Ontario
Canada

Contact Study Team

Primary Contact

Rose Raizman, NP, N-EC, PHCNP, NSWOC, WOCC

[email protected]
416-281-7111
The Mayer Institute
The Mayer Institute
Hamilton, Ontario
Canada

Contact Study Team

Primary Contact

Perry Mayer, MD, BSc, FFPMRCPS (Glasg)

[email protected]
905-523-1444
Study Sponsored By
MolecuLight Inc.
Participants Required
More Information
Study ID: NCT06682923