Ischemia Detection During Development of Acute Compartment Syndrome (NCT06079255) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Ischemia Detection During Development of Acute Compartment Syndrome
Norway60 participantsStarted 2025-10-15
Plain-language summary
This is an open, observational, prospective, descriptive, single-centre study including 60 patients. The study is designed to investigate if IscAlert sensor system can be used for reliable and continuous tissue carbon dioxide (pCO2)- and temperature monitoring in muscular tissue in lower extremity in patients at risk of developing acute compartment syndrome.
Who can participate
Age range18 Years – 110 Years
SexALL
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Inclusion Criteria:
* Must have a leg fracture that, perceived by the clinician, could give rise to later developing acute compartment syndrome condition.
* Subject must be 18 years or more.
* Able to sign informed consent.
* Expected cooperation of the patients for the treatment and follow up
Exclusion Criteria:
* Another study interfering with current study
* Any reason why, in the opinion of the investigator, the patient should not participate.
* Patients where a fasciotomy has already been decided should be performed