The purpose of this post-market, observational study is to collect data under anticipated conditions of use that demonstrates that DEXTER performs as intended in the intended patient population, including a variety of representative disease etiologies and demographic groups.
Study Type
OBSERVATIONAL
Enrollment
140
Robotic-assisted inguinal hernia repair with the DEXTER robotic surgery system
Northtowns Ambulatory Surgical Center (NASC)
Buffalo, New York, United States
RECRUITINGMemorial Hermann-Texas Medical Center - UT Health Houston
Houston, Texas, United States
RECRUITINGPrimary safety outcome
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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