Evaluation of Intravascular Monitoring of Partial PRessure of Oxygen for Neonatal intensiVE Care Patients
- Conditions
- Newborn, Infant, DiseaseCathetersOxygen Saturation
- Interventions
- Device: Neosense Umbilical Catheter
- Registration Number
- NCT03967587
- Lead Sponsor
- Neosense Technologies
- Brief Summary
The study is a non-blinded trial with one single intervention in sick newborn infants. The Neosense umbilical catheter will be used instead of the routinely used umbilical catheter on infants where the treating physician has ordered use of an umbilical catheter. The catheter will be connected to the Neosense monitor/measuring unit.
Blood samples for blood gas analysis are collected from the patients according to the clinical routine (every 4th to 6th hour). Oxygen tension data from the Neosense measuring system, from the time points when a blood gas sample was collected, will be recorded. This data will be compared to the oxygen tension value from the blood gas sample collected at the same time point. The blood gas samples will be analysed according to clinical and laboratory routine.
The infants will remain in the study as long as the Neosense measuring system is used.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 6
-
Sick newborn infants where the clinical routine indicates use of an umbilical catheter. At least one of the criteria below should be fulfilled:
- The infant needs invasive measurement of blood pressure.
- The infant needs repetitive sampling of blood.
- The infant needs prolonged infusion(s) > 2 days.
- The infant needs infusion of vessel irritating and potentially vessel harming solutions.
- The infant is born extremely preterm (before 28+0 weeks gestational age).
- A newborn infant with severe respiratory disorder, requiring oxygen treatment (more than 40% Fraction of inspired oxygen (FiO2)).
- The infant is undergoing therapeutic hypothermia following asphyxia ("oxygen deficiency at birth").
- The infant has a severe infection/sepsis.
-
Signed informed consent form by both parents (or guardians), (if the infant has only one parent (or guardian) one informed consent is required).
Exclusion criteria:
- Gastroschisis
- Omphalocele
- Peritonitis
- Necrotizing enterocolitis
- Omphalitis
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Neosense Umbilical Catheter Neosense Umbilical Catheter -
- Primary Outcome Measures
Name Time Method Measurement performance of an intravascular oxygen sensor in the Neosense system. Average of measurement comparisons done at every blood gas sample, i.e. every 4th - 6th hour during the study (up to 8 days) The oxygen tension measured by the Neosense system, compared to the oxygen tension measured by a blood gas analyser.
- Secondary Outcome Measures
Name Time Method Any deviations from normal procedures when inserting an umbilical catheter. During day 1 Number of attempts to place the catheter for each patient. Any accessories needed to introduce or handle the Neosense catheter.
Clinical complications with the Neosense catheter. During study, up to 8 days The number of occasions when the Neosense catheter had to be removed and the underlying reason. This includes all anticipated device effects as well as placing the catheter in the wrong vessel, impossible to measure blood pressure, collect blood samples and/or administer fluids.
Number of monitor lockups or battery depletions During study, in average 4-5 days Timepoint for monitor lockup or battery depletion, in case of occurrence.
Usability and functionality of the Neosense monitor. During study, in average 4-5 days Occurence of anticipated adverse device effects for the monitor.
Trial Locations
- Locations (2)
Karolinska University Hospital
🇸🇪Huddinge, Sweden
Uppsala University Children's Hospital
🇸🇪Uppsala, Sweden