- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07643545
Mitochondrial Energy Metabolism in Burns (Mito Burn)
The Role of the Mitochondrian in the Metabolic Stress Response to Burn Trauma
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.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Craig Porter, PhD
- Phone Number: 5013643340
- Email: cporter@uams.edu
Study Contact Backup
- Name: Lily Cheak, B.S.
- Phone Number: 5013643340
- Email: lcheak@uams.edu
Study Locations
-
-
Arkansas
-
Little Rock, Arkansas, United States, 72202
- Recruiting
- Arkansas Children's Hospital
-
Principal Investigator:
- Craig Porter, PhD
-
Sub-Investigator:
- Esther Teo, MD
-
Sub-Investigator:
- Robert Maxson, MD
-
Sub-Investigator:
- Richard Yeager, MD
-
Sub-Investigator:
- Daniel Lozano, MD
-
Sub-Investigator:
- Mandy Yelvington, MS, OTR/L
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood Bioenergetics
Time Frame: Through study completion, an average of 1 year
|
Peripheral Blood Mononuclear Cell (PBMC) respiration
|
Through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood metabolics signatures
Time Frame: Through study completion, an average of 1 year
|
Peripheral Blood Mononuclear Cell (PBMC) respiration
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Craig Porter, PhD, Arkansas Children's Research Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 263136
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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