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Clinical Trials/NL-OMON53891
NL-OMON53891
Not Yet Recruiting
N/A

Clinical validation study of a wireless and wearable sensor for continuous vital signs monitoring in a clinical setting with vital sign ranges limited to the parameters recorded in a post anesthesia care unit - Clinical performance of a new wearable vital signs monitoring device

Fastfocus BV0 sites20 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Fastfocus BV
Enrollment
20
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Fastfocus BV

Eligibility Criteria

Inclusion Criteria

  • Adult patients (\>18 years) (all sexes)
  • Surgical admission to hospital
  • At risk for transient perioperative desaturation (intermediate and major
  • Minimum expected duration at the recovery: at least 12 hours
  • (excluding day case surgery)

Exclusion Criteria

  • Inability to give informed consent.
  • Planned primary post\-operative admission to the Intensive Care Unit
  • Surgical location on \- or close \- to the ear
  • Patients with any of the contraindications (see section 4\.3\.1 of protocol
  • pagina 13\)
  • Pregnant or breastfeeding women

Outcomes

Primary Outcomes

Not specified

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