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Improving Female Sexual Wellness

NCT04824820 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2023-04-06

No results posted yet for this study

Summary

The purpose of this study is to assess the effect of commercially available genital vibrator use on sexual health, female pelvic floor disorders, and overall quality of life among a diverse population of women.

Conditions

  • Sexuality
  • Sexual Dysfunction
  • Sexual Desire Disorder
  • Hypoactive Sexual Desire Disorder
  • Orgasmic Disorder
  • Pelvic Organ Prolapse
  • Urinary Incontinence
  • Interstitial Cystitis
  • Pelvic Floor Disorders
  • Female Sexual Dysfunction

Interventions

BEHAVIORAL

Vibrator

Clitoral stimulation

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    lead OTHER

Principal Investigators

  • Karyn Eilber, MD · Cedars-Sinai Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-10
Primary Completion
2023-01-01
Completion
2023-04-05

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT04824820 on ClinicalTrials.gov