Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Stress Urinary Incontinence
  • Vulvovaginal Signs and Symptoms
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Eligible subjects will receive 1 treatment with the MorpheusV Applicator according to the study protocol.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 35 years and 75 years
Gender
Only males

Description

The objective of this trial is to evaluate the safety and efficacy of the MorpheusV Applicator for Symptoms of Stress Urinary Incontinence and Vulvovaginal Atrophy

The objective of this trial is to evaluate the safety and efficacy of the MorpheusV Applicator for Symptoms of Stress Urinary Incontinence and Vulvovaginal Atrophy

Tracking Information

NCT #
NCT04705571
Collaborators
Not Provided
Investigators
Principal Investigator: Tracy Blusewicz, MD Advanced Women's Care of the Lowcountry, PC