Ireland
--:--IST
Latest
Clinical Trials in Norway / NCT05297266
Active, not recruiting Not applicable

Early Discovery of Ischemia After Replantation Surgery of the Extremities

NCT05297266 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2022-11-15
Last updated
2026-04-28

Condition(s) studied

IschemiaBlood Circulation DisorderCarbon DioxideBiosensing TechniquesAmputation, Traumatic

Investigational drug(s) / intervention(s)

IscAlert

IscAlert: Insertion of a CO2- and temperature sensor in the distal part of the replanted extremity

Study summary

Investigators will test if changes in CO2 is detected postoperatively in ischemic tissue in a replanted extremity of a traumatically amputated upper or lower extremity. IscAlert is measuring continuously CO2 in muscular and subcutaneous tissue. IscAlert is inserted distal to the operative field into normal muscle and/or subcutaneous tissue in the replanted extremity. Local tissue CO2 and temperature will be monitored continuously postoperatively for the next 10 days. If a reduced or totally obstructed blood flow appear (thrombosis), an increase in tissue CO2 and a lower local temperature will emerge rapidly as a sign of ischemia. This will be detected by the sensor which will alarm the investigators. This will lead to assessment of the replanted extremity and if restricted blood flow is diagnosed, a reoperation will be performed. After reoperation new sensors will be implanted for another ten days if applicable. Sixty patients will be enrolled to undergo the procedures. The IscAlert will be removed from the patient before the patient is discharged from the hospital or a maximum of 10 days (the event that occurs first). 500 devices is planned to be used in this clinical study.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Patients must be in need of extremity replantation surgery * Subject must be ≥ 18 years * Able to give written signed informed consent Exclusion Criteria: * None

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Oslo University Hospital Oslo Norway

More Oslo University Hospital trials in Norway

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05297266 on ClinicalTrials.gov ↗ ← All trials in Norway