The aim of this clinical investigation is to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing incisional or primary ventral hernia repair.
Study Type
OBSERVATIONAL
Enrollment
33
Robotic-assisted incisional or primary ventral hernia repair with the DEXTER robotic surgery system
Allgemein öffentliches Krankenhaus Spittal/Drau
Spittal an der Drau, Austria
GH Saintes - Saint-Jean-d'Angély Site de Saintes
Saintes, France
Artemed Klinikum München Süd
München, Germany
Kantonsspital Winterthur
Winterthur, Switzerland
Primary safety 0utcome
Occurrence of Clavien-Dindo grades III-V adverse events
Time frame: up to 30 days after surgery
Primary efficacy outcome
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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Hirslanden Klinik Zürich
Zurich, Switzerland