This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing robotic-assisted and laparoscopic cholecystectomy.
Study Type
OBSERVATIONAL
Enrollment
51
Robotic-assisted and laparoscopic cholecystectomy
Groupe Hospitalier Saintes - Saint-Jean-d'Angély
Saintes, France
Universitätsklinikum Bonn
Bonn, Germany
Kantonsspital Winterthur
Winterthur, Switzerland
Klinik Hirslanden Zürich
Zurich, Switzerland
primary safety endpoint
occurrence of Clavien - Dindo grades III-V adverse events
Time frame: up to 30 days
primary performance endpoint
successful completion of the Dexter-assisted procedure, i.e. free of any conversion to an open or fully laparoscopic surgical approach
Time frame: intraoperative
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