Anovo™ Surgical System - Registry Study
ConditionGYN Disorders
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorMomentis Surgical
About this trial
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 criteria
Qualifiers
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
Disqualifiers
None
Trial design
Treatments tested in this trial
- anovo™ Surgical System
Treatment groups
300 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov