Anovo™ Surgical System - Registry Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
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
Participation Requirements
Sex: Female
Healthy Volunteers: t
View:

• 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

Locations
United States
Florida
AdventHealth
RECRUITING
Celebration
Contact Information
Primary
Sharon H Branch
sharon.branch@momentissurgical.com
9543033777
Backup
Matthew McKittrick
matthew.mckittrick@momentissurgical.com
6106745544
Time Frame
Start Date: 2023-06-28
Estimated Completion Date: 2026-06
Participants
Target number of participants: 300
Treatments
Patients undergoing gynecological surgical procedure with the anovo Surgical System
Related Therapeutic Areas
Sponsors
Leads: Momentis Surgical

This content was sourced from clinicaltrials.gov