Trials / Recruiting
RecruitingNCT06457971
Anovo Surgical System in Ventral Hernia
Clinical Assessment Protocol: Anovo Surgical System in Ventral Hernia
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Momentis Surgical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The study is aimed to clinically assess the AnovoTM Surgical System in ventral hernia procedures. Extensive preclinical testing of the system's integrity and safety has been performed to assure adequate safety for this trial.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Robotic Ventral Hernia Repair | The AnovoTM Surgical System is an endoscopic instrument control system that is intended to assist in the accurate control of the Instrument ARMS with graspers and electrosurgery devices for endoscopic manipulation of tissue including grasping, blunt dissection, approximation, and electrosurgery, during single site, laparoscopic surgical procedures. The AnovoTM System's articulated robotic arms allow the surgeon to access and reach different structures in the pelvic and abdominal cavity. Closing the fascial defect robotically is easier from a technical standpoint than attempting it with classical laparoscopic instruments |
Timeline
- Start date
- 2024-01-14
- Primary completion
- 2025-12-01
- Completion
- 2025-12-01
- First posted
- 2024-06-13
- Last updated
- 2024-11-21
Locations
2 sites across 2 countries: Belgium, Israel
Source: ClinicalTrials.gov record NCT06457971. Inclusion in this directory is not an endorsement.