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Anovo™ Surgical System - Registry Study

Anovo™ Surgical System - Registry Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05945433
Enrollment
300
Registered
2023-07-14
Start date
2023-06-28
Completion date
2026-06-30
Last updated
2023-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

GYN Disorders

Brief 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).

Detailed description

Specific Aims: 1. To collect RWD from surgeons with varying experience and expertise on their learning curve and time to achieve competency, and as such assess the success of the Skills Development Pathway. 2. Collect safety information and analyze the causality between type and frequency of adverse events to surgeons' experience. 3. Evaluate the effectiveness of the device while minimizing bias by enrolling all comers, which will represent the general patient population.

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.

Sponsors

Momentis Surgical
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

All patients receiving gynecological surgical procedure with the anovo Surgical System by their surgeon will be offered to participate in the registry. Inclusion Criteria: * 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 criteria

-none

Design outcomes

Primary

MeasureTime frame
Rate of Unanticipated Adverse Device Effect8 Weeks Follow Up
Conversion rate to open or laparoscopic approachProcedure

Secondary

MeasureTime frame
Surgery time (minutes)Procedure

Other

MeasureTime frameDescription
Surgeon Learning Curve (surgery time against number of operations performed, considering frequency of cases and surgery difficulty)ProcedureTo be reported as a continuous curve (plot per surgeon), and as the mean difference in surgery times between during learning curve and after learning curve stages (stages defined as before the surgeon achieves a steady state surgical time and after the surgeon achieves the steady state)
Surgeon Safety Curve (cumulative UADEs against number of operations performed)Procedure
User Skills Development SurveyProcedure

Countries

United States

Contacts

Primary ContactSharon H Branch
sharon.branch@momentissurgical.com9543033777
Backup ContactMatthew McKittrick
matthew.mckittrick@momentissurgical.com6106745544

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026