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A Long-term Evaluation of a Novel Intravaginal Device

NCT03073824 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 65

Last updated 2018-12-03

No results posted yet for this study

Summary

An open-label long-term evaluation of a novel intravaginal device in female patients experiencing sexual and bladder function issues.

Conditions

  • Pelvic Floor Disorders
  • Sexual Dysfunction
  • Stress Incontinence

Interventions

DEVICE

vSculpt

Pelvic Floor Toning and Vaginal Rejuvenation Device

Sponsors & Collaborators

  • Joylux, Inc.

    lead OTHER

Principal Investigators

  • Sarah De La Torre, MD · Seattle OB/GYN Group

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
59 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-06
Primary Completion
2018-11-29
Completion
2018-11-29

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 NCT03073824 on ClinicalTrials.gov