Hugo Robotic Assisted Surgery in Inguinal and Ventral Hernia Repair Surgery - Clinical Trial
What is the Purpose of this Study?
We are doing this study to evaluate the safety and performance of a medical technology called the Medtronic Hugo® RAS system (the study device) in hernia repair robotic assisted surgery (RAS) procedures.
What is the Condition Being Studied?
Hernia
Who Can Participate in the Study?
Adults ages 22+ who are scheduled to have an inguinal or ventral robotic hernia procedure.
For more information, contact the study team at shawn.greene@duke.edu.
Age Group
Adults
What is Involved?
If you choose to join this study, it will include up to 6 visits:
- A screening visit to make sure you are eligible to take part
- A surgical visit to have your procedure with the study device
- A 30-day follow-up visit to see how you are doing
- A 3-month follow-up visit to see how you are doing
- A 1 year follow-up visit to see how you are doing
- A 2 year follow-up visit to see how you are doing
Study Details
Full Title
A prospective, multi-center, single-arm study of the Medtronic HugoTM Robotic Assisted Surgery (RAS) System in Inguinal and Ventral Hernia Repair Surgery
Principal Investigator
Gastrointestinal Surgeon
Protocol Number
IRB:
PRO00114154
NCT:
NCT06445504
Phase
Phase
N/A
ClinicalTrials.gov
View on ClinicalTrials.gov
Enrollment Status
Open for Enrollment