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Recruiting NCT07643545

Mitochondrial Energy Metabolism in Burns

Observational Burn Injury

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Burn Injury. Basic parameters: 2 years — 80 years · 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 →
Official title

The Role of the Mitochondrian in the Metabolic Stress Response to Burn Trauma

Overview

The goal of this observational study is to assess the impact of burn injury on cellular energetics in patients that have been admitted to the burn center at Arkansas Children's Hospital for burn care and require one or more procedures to clean, debride, and repair burn wounds will be eligible to participate in this study. During the study, we will collect the following information: * General background information such as date of birth, height, weight, and other basic information. * Medical information, such as: basic medical information, details of burn injury, vital signs on the day of surgery, medicines you take during your stay, and some clinical tests. * Blood, urine, and tissue during surgeries you have during your stay.

Primary outcome measures

  • Blood Bioenergetics [Time frame: Through study completion, an average of 1 year]
Secondary outcome measures (1)
  • Blood metabolics signatures [Time frame: Through study completion, an average of 1 year]

Eligibility criteria

Inclusion criteria

  • Male or Female
  • Ages 2 years to 80 years
  • Requiring hospital admission for burn care
  • All races
  • All ethnicities

Exclusion criteria

  • Age < 2 years
  • Under 10 kg in body mass
  • Age > 80 years
  • Active pregnancy
  • Unable to provide informed consent and no legal authorized representative present
  • Patient is considered moribund at the time of admission by the treating physician.

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
  • Arkansas Children's Hospital — Little Rock

Identifiers

NCT: NCT07643545 · 263136

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗