Status:
COMPLETED
Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM
Lead Sponsor:
The Cleveland Clinic
Collaborating Sponsors:
Intuitive Surgical
Conditions:
Ventral Hernia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The investigators aim to conduct a registry-based, randomized controlled trial to investigate if the robotic platform for minimally invasive ventral hernia repair with intraperitoneal onlay mesh (IPOM...
Detailed Description
Despite the adoption of the robotic platform for ventral hernia repair, there is still a paucity of literature to speak to the benefits of this approach. In a recently-published propensity score analy...
Eligibility Criteria
Inclusion
- Adult patients (\>18 years old)
- Primary or Incisional Ventral Hernia
- Midline defect location
- H. Width equal or less than 7 centimeters
- Elective setting
- Able to give informed consent
- Able to tolerate general anesthesia
- Considered eligible for minimally invasive ventral hernia repair
- Willing to undergo mesh-based repair
- Fascial closure is presumed to be achieved
Exclusion
- Younger than 18 years old
- Non-midline hernia defects
- H. Width \> 7cm
- Emergent setting ( acute incarceration or strangulation)
- Unable to give informed consent
- Unable to tolerate general anesthesia
- Considered not eligible for minimally invasive ventral hernia repair
- Not willing to undergo mesh based repair
- Fascial closure not intended or presumed not to be achieved
Key Trial Info
Start Date :
September 11 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 31 2021
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT03283982
Start Date
September 11 2017
End Date
January 31 2021
Last Update
July 25 2022
Active Locations (1)
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1
Cleveland Clinic Comprehensive Hernia Center
Cleveland, Ohio, United States, 44195