RecruitingAtrophic VaginitisVaginal AtrophyGenitourinary Syndrome of Menopause
VALOR: Vaginal Atrophy & Long-term Observation of Recovery
Eligible age
18+ yrs
Accepts
Women
Locations
9 states
Healthy volunteers
No
See if you qualify for this study
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About this study
Vulvovaginal skin conditions, namely vaginal atrophy, lichen sclerosus, lichen simplex chronicus and lichen planus affecting the female adult population will be treated with a novel gel dressing to test the short- and long-term safety and efficacy of the device.
Sponsor: Stratpharma AG
You may qualify if…
- ✓ Diagnosed atrophic vaginitis, lichen sclerosus, lichen simplex chronicus or lichen planus
- ✓ Continuous vulvovaginal symptoms
- ✓ Access to smartphone and tablet, laptop or computer
- ✓ Access to a valid email address
You may not qualify if…
- ✕ Unable to provide informed consent
- ✕ Patient unable to apply topical device
- ✕ Allergy or intolerance to ingredients or excipients of the formulation of studied products
- ✕ Systemic hormonal therapy started less than 30 days before baseline
- ✕ Systemic corticosteroids ongoing treatment or used within the last 30 days before baseline
- ✕ Ongoing topical HRT or corticosteroid treatment for the indication under investigation
- ✕ Topical HRT or corticosteroid treatment used for the indication under investigation within the last 30 days before baseline
Where it's recruiting
Alabama
Birmingham
California
Burbank · Laguna Hills · Los Alamitos · Newport Beach …
Florida
Lake City
Georgia
Sandy Springs
Nevada
Las Vegas
North Carolina
Fayetteville
South Carolina
Charleston · West Columbia
Tennessee
Memphis
Texas
Dallas
Source: ClinicalTrials.gov · NCT05953090 · last updated 2026-02-20