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Recruiting NCT01166893

Ability of Modulated Imaging and Laser Speckle Imaging to Determine Burn Wound Severity and Healing Potential

Observational Skin Burn Multiple

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Modulated Imaging and Laser Speckle Imaging.
Who it may be relevant to
Registry conditions: Skin Burn Multiple. Basic parameters: from 1 Minute · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

According to the National Burn Repository 2007, the most common type of burn injury is a partial thickness burns. The current standard of care for partial thickness burns is two weeks of topical therapy and wound care. Burns that do not heal within two weeks undergo surgical excision and skin grafting.

Detailed description

Researcher can use the combination of Modulated Imaging and Laser Speckle Imaging can be used as an adjuvant to standard clinical evaluation to gauge burn wound and severity of infection. Researcher can image the burn wounds of and compare with current standard of care, clinical exam, and can use the outcomes information in terms of time to healing and treatment

Modulating Imaging is a noninvasive optical modality measure the metabolic functions of the burn wound.

Laser Speckle Imaging is a noninvasive optical modality can measure blood flow of burn wound.

Interventions

  • Device Modulated Imaging and Laser Speckle Imaging
    wound healing

Primary outcome measures

  • Noninvasive burn wound severity assessment [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • Male / female all age
  • Subjects is an inpatient or out patient with burn wound

Exclusion criteria

  • Subjects cannot lied flat and still for the duration of the imaging
  • Subjects pregnant.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • UCIMC — Orange

Identifiers

NCT: NCT01166893 · 20097322 · R01GM108634

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗