VALOR: Vaginal Atrophy & Long-term Observation of Recovery
Status: Recruiting
Location: See all (12) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:
• 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
Locations
United States
California
Orange Coast Women's Medical Group
ACTIVE_NOT_RECRUITING
Laguna Hills
WR-PRI, LLC (Los Alamitos)
NOT_YET_RECRUITING
Los Alamitos
WR-PRI, LLC (Newport Beach)
RECRUITING
Newport Beach
WR-Women's Health Care Research, LLC
NOT_YET_RECRUITING
San Diego
Florida
WR-Multi-Specialty Research Associates
NOT_YET_RECRUITING
Lake City
Georgia
WR-Mount Vernon Clinical Research, LLC
NOT_YET_RECRUITING
Sandy Springs
North Carolina
WR-Carolina Institute for Clinical Research
RECRUITING
Fayetteville
Nevada
WR-Clinical Research Center of Nevada, LLC
NOT_YET_RECRUITING
Las Vegas
South Carolina
WR-Charleston Clinical Trials, LLC
NOT_YET_RECRUITING
Charleston
Southern Urogynecology
RECRUITING
West Columbia
Tennessee
WR-Medical Research Center of Memphis, LLC
NOT_YET_RECRUITING
Memphis
Texas
WR-Global Medical Research, LLC
RECRUITING
Dallas
Time Frame
Start Date: 2023-10-30
Estimated Completion Date: 2026-12
Participants
Target number of participants: 2000
Treatments
Experimental: Feasibility
Related Therapeutic Areas
Sponsors
Leads: Stratpharma AG