About this trial

This study evaluates the efficacy and safety of Artisential laparoscopic instruments in minimally invasive gynecologic surgery.

Eligibility criteria

Qualifiers

Patient scheduled for robotic or laparoscopic total hysterectomy

Patient scheduled for robotic or laparoscopic sacrocolpopexy

Disqualifiers

Not a candidate for the above surgical procedures

Trial design

Treatments tested in this trial

  • Articulating laparoscopic instrument
  • Conventional laparoscopic instrument
  • Robotic surgical instrument

Treatment groups

50 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Kern Medical Center

Lead sponsor

Livs Med

Collaborator