Finished
Evaluation of Clinical Outcomes in Robotic-Assisted Inguinal Hernia Repair
NCT02684448 · Intuitive Surgical · Updated 28 March 2017
- What is being tested
- Inguinal Hernia Repair
- For
- Hernia, Inguinal; Hernia, Inguinal, Direct; Hernia, Inguinal, Indirect
- Kind of study
- Watches patients without assigning a treatment. No drug phase (a device or procedure study).
- Who can join
- Ages 18 years and older. About 1,258 people. The full rules are on the registry page.
- Where
- United States (2 sites)
- When
- Starts or started Jan 2016, ends Jan 2017. Registered 18 Feb 2016.
- Results
- None posted yet.
In the researchers' words
This multi-center, retrospective data collection study will evaluate the feasibility, safety and performance of the da Vinci® surgical system for patients who have undergone robotic-assisted inguinal hernia repair, as well as provide information about the learning curve associated with robotic-assisted (da Vinci®) inguinal hernia repair. In addition, this retrospective data collection study will evaluate the perioperative outcomes of robotic-assisted (da Vinci®) inguinal hernia repair and compare perioperative outcomes with those associated with open hernia repair by the same participating surgeon.
Sites
- Progressive Surgical Associates/Silver Cross HospitalNew Lenox, Illinois, United States
- Rochester General HospitalRochester, New York, United States