- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03876340
Impact of a Clinical Decision Algorithm on Length of Hospital Stay and Costs of Care of Burned Patients
Impact of a Clinical Decision Algorithm on Length of Hospital Stay and Costs of Care of Burned Patients: a Pragmatic Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Burn wounds are divided into first degree burns involving the epidermis, superficial second degree with lesion of the papillary dermis, deep second degree with lesion of the reticular dermis, third degree with lesion to the hypodermis, and fourth degree involves fascia, muscle, tendons and bone.
In burns, development and severity of complications are in direct proportion to the magnitude of the burn. The magnitude of the damage depends on three factors, the duration of the contact, the intensity of the current or temperature and the resistance offered by the tissue. The extent of the burned skin surface is very useful to assess the severity of the patient, it is a relevant criterion to develop the prognosis. It is important to have comprehensive knowledge of the burned patient and close collaboration with the multidisciplinary care team through a careful evaluation that includes mechanism of injury, type, extent, degree of affectation and organic repercussion of the burn. The reliable and valid evaluation on the depth of a burn wound or the healing potential is essential for the decision making in the treatment; to provide a prognosis and to compare the different treatment modalities. There is no gold standard in the evaluation of burns.
Infrared imaging is a non-invasive technique that quantifies the temperature of the body surface by capturing the thermal radiation emitted and producing a high-resolution digital image called a thermogram. The presence of a disease interferes locally with the heat balance, which results in an increase or decrease in the temperature of the skin, in comparison to the surrounding regions or the contralateral not affected region. A degree of thermal asymmetry between opposite sides of the body (ΔT) of up to 1 ° C has been considered indicative of dysfunction. In several previous studies the parameters of initial thermography between the wound and healthy skin (delta T) were defined, to decide the therapeutic approach of the burns to predict the evolution: ΔT <3º C epithelialized with conservative treatment, ΔT 3-5º C should be graft early and ΔT> 5º C should be amputated.Thermography offers a feasible option for valuation.
Methods:
This is randomized clinical study of patients with different burn depth. All patients will be examined using a thermal camera.
Expected Results:
In all cases, the investigators obtained infrared images that corroborate clinical findings.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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San Luis Potosi, Mexico, 78290
- Hospital Central Dr. Ignacio Morones Prieto
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with partial or full thickness burn in <15% of the total body surface area in distal limbs, including hands or feet.
- Patients admitted to the burn care unit within 24 hours from injury.
- Patients that signed the informed consent. In the case of children or patients unable to consent themselves, signing of the consent by their guardian.
Exclusion Criteria:
- Patients who sustained electrical burns.
- Patients that received previous care in any other unit.
- Patients with uncontrolled chronic diseases.
- Patients that used corticosteroids or cytotoxic medications within 3 months of sustaining the injury.
- Patients with a baseline body mass index of <19.9 for adults or below the 5th percentile for their age in children.
- Presence of foreign bodies embedded in the wound tissue, gross edema, systemic causes of distal hypoperfusion, or presence of local infection.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Current treatment
Patients will receive burn care treatment as dictated by the surgical team (current standard of care).
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Digital infrared thermograms will be obtained during the first contact with the patients.
Temperature recordings of the injured and healthy skin will be used to calculate the temperature difference between the structures, but the results will be kept sealed until the study is finished.
The patients will receive the usual standard of care as dictated by the surgical team.
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EXPERIMENTAL: Algorithm-dictated treatment
Patients will receive burn care treatment as dictated by the treatment algorithm (PLOS ONE 13(11): e0206477.).
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Digital infrared thermograms will be obtained during the first contact with the patients.
Temperature recordings of the injured and healthy skin will be used to calculate the temperature difference between the structures.
The thermograms will be used to dictate the initial treatment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Length of stay
Time Frame: Through study completion, an average of 30 days
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Number of days the patient stays in the burn care unit
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Through study completion, an average of 30 days
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Treatment modality conversion
Time Frame: Through study completion, an average of 30 days
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Change of the initial treatment modality
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Through study completion, an average of 30 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Rate of complications
Time Frame: Through study completion, an average of 30 days
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Presence of complications such as tissue necrosis, infection, death.
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Through study completion, an average of 30 days
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Cost of stay
Time Frame: Through study completion, an average of 30 days
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Total cost of the stay in the burn care unit in american dollars (USD)
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Through study completion, an average of 30 days
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Collaborators and Investigators
Investigators
- Study Chair: Jose L Ramirez Garcia Luna, MD, MSc, Universidad Autonoma de San Luis Potosí
Publications and helpful links
General Publications
- Martinez-Jimenez MA, Ramirez-GarciaLuna JL, Kolosovas-Machuca ES, Drager J, Gonzalez FJ. Development and validation of an algorithm to predict the treatment modality of burn wounds using thermographic scans: Prospective cohort study. PLoS One. 2018 Nov 14;13(11):e0206477. doi: 10.1371/journal.pone.0206477. eCollection 2018.
- Medina-Preciado JD, Kolosovas-Machuca ES, Velez-Gomez E, Miranda-Altamirano A, Gonzalez FJ. Noninvasive determination of burn depth in children by digital infrared thermal imaging. J Biomed Opt. 2013 Jun;18(6):061204. doi: 10.1117/1.JBO.18.6.061204.
- Kolosovas-Machuca ES, Gonzalez FJ. Distribution of skin temperature in Mexican children. Skin Res Technol. 2011 Aug;17(3):326-31. doi: 10.1111/j.1600-0846.2011.00501.x. Epub 2011 Feb 22.
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- QX2018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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