Retrospective Chart Review Study of Patients Treated With Votiva Device

NCT04437680 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2022-01-11

No results posted yet for this study

Summary

retrospective data collection is to gain insight into patients satisfaction post Votiva treatments for the complex of vulvovaginal symptoms.

Conditions

  • Vulvovaginal Signs and Symptoms

Interventions

DEVICE

Votiva device

A retrospective chart review of the medical records

Sponsors & Collaborators

  • InMode MD Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-05
Primary Completion
2020-12-30
Completion
2020-12-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04437680 on ClinicalTrials.gov