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N/A
Burn: blood collection for Burns
N/A
Waitlist Available
Led By Jon Simmons, MD
Research Sponsored by University of South Alabama
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 1 year to assess outcome measure
Awards & highlights
Study Summary
This trial will study whether or not levels of mitochondrial dysfunction can be measured in the blood and whether or not this is a predictor of organ failure in burn and trauma patients.
Eligible Conditions
- Burns
- Trauma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 1 year to assess outcome measure
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 1 year to assess outcome measure
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Plasma mtDNA DAMPs concentration
Trial Design
3Treatment groups
Experimental Treatment
Group I: trauma: blood collectionExperimental Treatment1 Intervention
blood to be collected at different time intervals. Blood draw as the intervention
Group II: healthy volunteers: blood collectionExperimental Treatment1 Intervention
Blood draws as the intervention
Group III: Burn: blood collectionExperimental Treatment1 Intervention
Procedure: Blood draws as the intervention.
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Who is running the clinical trial?
University of South AlabamaLead Sponsor
42 Previous Clinical Trials
15,884 Total Patients Enrolled
1 Trials studying Burns
Jon Simmons, MDPrincipal Investigator - University of South Alabama, Department of Surgery
University of South Alabama Medical Center, Usa Health Physician Billing Services Llc
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