Anovo Surgical System in Ventral Hernia
ConditionVentral Hernia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMomentis Surgical
About this trial
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.
Eligibility criteria
Qualifiers
Subject is at least 18 years old.
Subjects able to provide written informed consent.
Subject deemed eligible candidate by surgeon and will comply with the study procedures.
Subjects with ventral hernia.
Disqualifiers
Women who are pregnant or breast-feeding or who wish to become pregnant during the period of the clinical investigation.
Subject has medical condition, which in the judgement of the investigator makes the subject a poor candidate for the investigational procedure.
Participation in another clinical trial that is in the active phase.
Subject unwilling or inability to follow procedures outlined in the protocol.
Trial design
Treatments tested in this trial
- Robotic Ventral Hernia Repair
Treatment groups
50 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov