Clinical Research Directory

Inclusion Criteria: 1. Willing and able to give informed consent, have a witnessed verbal consent, family discussion if intubated and retrospective consent for those that are intubated 2. Life expectancy \> 1 month 3. Thermal burn mechanism (flame, scald, or contact) 4. The Study Burn(s) occurred less than 72 hours prior to the time of first imaging 5. Minimum burn wound size for adult or paediatric participants is 0.25% TBSA per region 6. Have burn(s) on the head, hands and/or feet that meet the criteria for a Study Burn. If multiple regions meet the Study Burn criteria, per the discretion of the Investigator, all Study Burn regions should be included. Exclusion Criteria: 1. Sepsis at the time of enrolment 2. Infection of the burn wound at the time of enrolment 3. Immunosuppression / radiation / chemotherapy \< 3 months prior to enrolment 4. Concurrent use of investigational products with a known effect on the burn sites; and/or imaging 5. Concurrent use of products such as chemical debriding agents, skin substitutes and others that the principal investigator deems will have an impact on the image quality and healing potential of a Study Burn 6. Any condition that, in the opinion of the Investigator, may prevent compliance with the study requirements or compromise Participant safety 7. Participants without a burn on the hands, feet, head or neck, or burns located on these regions only on the palmar or plantar surfaces 8. Chemical or any other non-thermal burns 8\. Participants anticipated to or undergoing enzymatic debridemen9