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.
Investigators
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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