Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Joylux, Inc.
To determine the long-term clinical efficacy of the vSculpt therapy on treating the pelvic floor area and vaginal tissue for females who experience bladder and sexual dysfunction.
Age
30–59
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
All study participants are required to be biological females (genotype XX) to participate
Female participants will be of adult age, over 18
Female participants with self-reported concerns with bladder and sexual function
Female participants who have reliable and consistent computer and internet access on a daily basis
You may not be if
Female participants shall not have an active sexually transmitted disease and/or infection
Female participants who are actively undergoing chemotherapy or radiation
Female participants who are currently taking any cancer-related or photosensitivity drugs
Female participants who are pregnant, who may think they are pregnant, and/or actively trying to get pregnant during the clinical study
