NCT05521958
Gene Expression in Lower Extremity Acute Traumatic Compartment Syndrome
Enrolling by Invitation
NAAges 18–90InterventionalUniversity of UtahInvestigator-initiated
~80 participants
Updated 2026-04-29 on ClinicalTrials.gov
What's tested:Acute injury without compartment syndromeAcute injury with compartment syndromeExertional compartment syndrome
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Myostatin (% increase)
Measured over Immediately after the muscle tissue harvest procedure.
Conditions
Where it's being run
1 sites across 1 statesUtah1
Study leadership
- Justin Haller, M.D. · PRINCIPAL_INVESTIGATOR · University of Utah Orthopaedics
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Eligibility criteria
Inclusion
Patient 18+ years of age. English speaking.
Patients with the clinical diagnosis of lower leg acute compartment syndrome secondary to tibial shaft or tibial plateau fracture.
Patients without clinical compartment syndrome undergoing operative intervention within 48 hours of injury for tibial shaft or tibial plateau fractures.
Patients with the clinical diagnosis of exertional compartment syndrome with planned surgical intervention.
Exclusion
Non-english speaking participants
What this trial measures
- Myostatin (% increase)Immediately after the muscle tissue harvest procedure.
The investigators primary marker of interest is myostatin. The investigators will determine the (%) increase in myostatin levels in muscle tissues between compartment syndrome patients versus fracture controls. (%) increase in myostatin levels in muscle tissues between compartment syndrome patients versus patients with exertional compartment syndrome will also be determined. The measurement tool is polymerase chain reaction (PCR).