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Clinical Trials/NL-OMON50879
NL-OMON50879
Completed
Not Applicable

Supporting early recognition of clinical deterioration for Mobile Vital signs monitoring of high-risk surgical patients - MoViSupport

Ziekenhuisgroep Twente0 sites80 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Ziekenhuisgroep Twente
Enrollment
80
Status
Completed
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
Ziekenhuisgroep Twente

Eligibility Criteria

Inclusion Criteria

  • The study population includes two patient groups:
  • 1\. Patients aged (18 years and older) undergoing elective surgery for resection
  • of malignant
  • tumors of the upper gastrointestinal tract (upper GI patients)
  • 2\. Patients aged (70 years and older) undergoing surgery for a hip fracture and
  • admitted to the
  • hospital for pre\- or postoperative care (hip fracture patients)

Exclusion Criteria

  • 1\. Contraindications for use of vital sign sensor patch (i.e. skin allergy,
  • implanted medical devices)
  • 2\. Contact isolation

Outcomes

Primary Outcomes

Not specified

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