About this trial
This study is a single-center, observational study designed to collect tissue spectrometric data related to tissue oxygenation.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults, age of 18 - 90 years
Scheduled for peripheral arterial bypass surgery.
Scheduled for proximal arterial reconstruction.
Ability and willingness to provide informed consent.
Disqualifiers
Inability to provide informed consent
Considered a vulnerable person according to the Finnish Medical Research Act (488/1999), Chapter 2, Sections 7, 9, and 10, including retarded persons, pregnant women, nursing mothers, prisoners, and forensic patients.
A known history of severe allergic reaction to nickel.
Trial population
A Helsinki University Hospital patient scheduled for a vascular surgical operation.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Observe changes in skeletal muscle tissue oxygenation
To observe the changes in skeletal muscle tissue oxygenation (combined hemoglobin/myoglobin saturation, %) measured by the SpectroCor Monitoring System during arterial clamping and restoration of limb perfusion. Continuous spectroscopic measurement of combined hemoglobin and myoglobin oxygen saturation in skeletal muscle of the operated limb, recorded from a SpectroCor Sensor placed in the distal wound before any arterial clamping. Saturation values are time-stamped against intraoperative events affecting limb perfusion (proximal arterial clamping, unclamping, graft revision) and compared with paired arterial and venous blood gas samples obtained before clamping and after restoration of blood flow.
Secondary outcomes
Incidence of adverse events, adverse device effects, and device deficiencies
Number and proportion of participants experiencing at least one adverse event (AE), adverse device effect (ADE), serious adverse event (SAE), serious adverse device effect (SADE), or unanticipated serious adverse device effect (USADE), and the number of device deficiencies (DD) recorded. Events are recorded from the time of sensor placement until discharge from hospital and assessed for causal relationship to the investigational device by the investigator. Anticipated device-related events include topical bleeding at the sensor attachment site, local tissue reaction associated with tissue glue fixation, and local infection at the insertion site.
Locations
Sponsors and contacts
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Spectrocor
Lead sponsor
Helsinki University Central Hospital
Collaborator
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