Association of Cytokines With the Development of Complications in Burn and Toxic Epidermal Necrolysis (TENS) Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

65 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-02

Study Completion Date

2022-12-31

Brief Summary

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This study will involve blood draws to test for specific cytokines. The study goal is to gain a better understanding of the role of inflammatory response in the development of specific complications in burn and TENS patients.

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Detailed Description

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Conditions

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Inflammatory Response Multi Organ Failure Nosocomial Infection Deep Vein Thrombosis

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Blood Draw

This study will involve blood draws to test for specific cytokines

Blood Draw

Intervention Type OTHER

This study will involve blood draws to test for specific cytokines

Interventions

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Blood Draw

This study will involve blood draws to test for specific cytokines

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* is ≥18 years of age
* has been admitted to the Joseph M. Still Burn Center at Doctors Hospital Augusta with a burn diagnosis, or TENS OR SJS diagnosis (confirmed or non-confirmed), with an expected length of stay to be at least 7 days
* the subject or their legally authorized representative is able to provide informed consent
* has a negative urine or serum pregnancy test at screening (if female and has potential for pregnancy)