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Clinical Trial Summary

Compartment syndrome remains a very serious complication of lower extremity trauma and/or procedural cases that involved lower or upper extremity surgery. This condition results in muscle death, chronic pain, infection, and possible amputation. Early diagnosis is essential to institute interventions to avoid complications. Unfortunately, the subjective pain of the patient remains the mainstay for diagnosis. A method or device is needed that would improve the investigator's ability to diagnose this potentially devastating condition. The purpose of this trial is to evaluate the safety and functionality of MY01, an investigational device that allows continuous monitoring of intracompartmental muscle pressure in patients at risk for developing acute compartment syndrome. This is a single centre, non-randomized, non-controlled, unblinded, prospective trial of the MY01 device. A cohort of 25 participants will be prospectively enrolled to document the performance of the device.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04012723
Study type Interventional
Source MY01 Inc.
Contact
Status Completed
Phase N/A
Start date November 17, 2020
Completion date March 30, 2023

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03880656 - BM-MNCs for Lower Extremity Compartment Syndrome Injury Phase 1