WARD VASC

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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