Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Nutromics
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Capable of providing informed consent OR has a Medical Treatment Decision Maker who can provide informed consent per the informed consent form (ICF).
Aged 18 years at time of enrolment.
Prescribed vancomycin treatment for intravenous administration (Cohort 1 only); vancomycin treatment duration expected to be ≥48 hours from time of enrolment.
Has a central or arterial catheter and/or a large-bore cannula, or is willing to have intermittent peripheral blood sampling.
You may not be if
Currently receiving an investigational drug or device that, in the Investigator's opinion, may affect participation in this trial.
History of allergic reactions to metals, plastics and adhesives which, in the opinion of the Study Investigators, would increase the risk of allergic reaction associated with the Device.
Dermatological (or other) condition, or fragile skin, which in the opinion of the Investigators would prevent application of the Nutromics Sensor Device.
Severe oedema or local swelling at the intended application site that would likely impair ISF sampling.
Immediate life-threatening instability where study procedures would interfere with urgent care (participant may be screened once stable).
Pregnant, lactating, planning to become pregnant, breastfeed, or donate ova.
