WARD Surgery Pilot
Study design
Observational study
Sample size
50 participants
Study sites
Rigshospitalet
Inclusion criteria
Adult patients (from 65 years of age) undergoing elective major abdominal cancer surgery with an estimated duration of >2 hours and with a preoperative sinus rythm.
Study procedures
Included patients were monitored with WARD equipment from after the surgery in the post anesthesia care unit (POTA) and up to 4 days postoperatively while hospitalized.
Primary outome
Cardiopulmonary micro events (vital parameter deviation) during the entire monitoring period.
Primary Investigator
Camilla Lundgreen Duus, MD
NCT
NCT03102619
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