RecruitingNCT05945433

Anovo™ Surgical System - Registry Study


Sponsor

Momentis Surgical

Enrollment

300 participants

Start Date

Jun 28, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

To collect Real-World Data (RWD) on the ongoing safety and effectiveness of the anovo Surgical system in transvaginal gynecological laparoscopic surgical procedures and to obtain information on the impact of the anovo Skills Development Pathway on user behavior and performance (where performance is measured by the learning curve of the surgeons and procedure outcomes).


Eligibility

Sex: FEMALE

Inclusion Criteria3

  • All patients receiving gynecological surgical procedure with the anovo Surgical System by their surgeon will be offered to participate in the registry.
  • patients must understand and sign the informed consent form, including data privacy authorization, indicating their consent to participate in the registry study.
  • willing to complete post-operative questionnaire

Exclusion Criteria1

  • none

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICEanovo™ Surgical System

The anovo Surgical System is an endoscopic instrument control system that is intended to assist in the accurate control of the Instrument ARMS during single site, natural orifice laparoscopic-assisted transvaginal benign surgical procedures.


Locations(1)

AdventHealth

Celebration, Florida, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05945433


Related Trials