WARD-VASC: Observational Study in Patients Undergoing Major Vascular Surgery
Study design
Observational study
Sample size
40 participants
Study sites
Rigshospitalet
Inclusion criteria
Adult (>18 years) patients undergoing major vascular surgery.
Study procedures
Included patients are monitored with WARD equipment from after surgery in the post anesthesia care unit (PACU) and up to 4 days postoperatively, while hospitalized.
Primary outome
Primary outcome is the amount and duration of physiological parameter deviations. Secondary outcome is the number of postoperative complications wihtin 30 days after surgery.
Primary Investigator
Jesper Mølgaard, PhD student
NCT
None