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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

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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