Clinical Trials Directory

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

TypeNameDescription
DEVICERobotic Ventral Hernia RepairThe 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.