WARD Surgery observational study
Study design
Observational study
Sample size
500 participants
Study sites
Rigshospitalet and Bispebjerg Hospital
Inclusion criteria
Adult patients (from 18 years of age) undergoing elective major abdominal cancer surgery.
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
Primary outcome is the amount and duration of physiological parameter deviations. Secondary outcomes is the number of postoperative complications within 30 days after surgery.
Primary Investigator
Camilla Haahr-Raunkjær, MD, PhD student
Jesper Mølgaard, MD, PhD student
NCT
NCT03491137