The goal of this interventional study is to compare the efficacy and safety of vaginal hyaluronic acid, arginine and liposome gel versus vaginal lubricant in the treatment of genitourinary syndrome of menopause in postmenopausal women. The main question it aims to answer is: Is vaginal hyaluronic acid, arginine and liposome gel more effective than vaginal lubricant in the treatment of genitourinary syndrome of menopause in postmenopausal women Participants will be randomized into 2 treatment groups: vaginal hyaluronic acid, arginine and liposome group and vaginal lubricant group. Researchers will compare whether vaginal hyaluronic acid, arginine and liposome group has better improvement than vaginal lubricant group.
Age range
40 Years – 80 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
The change in VHI Questionnaire score
Timeframe: The change in VHI Questionnaire score is assessed at the baseline visit and at 12 weeks of vaginal gel/ vaginal lubricant application
The change in Vaginal Health Index (VHI)
Timeframe: The change in Vaginal Health Index (VHI) is assessed at the baseline visit and at 12 weeks of vaginal gel/ vaginal lubricant application
The change in Vaginal Maturation Index (VMI)
Timeframe: The change in Vaginal Maturation Index (VMI) is assessed at the baseline visit and at 12 weeks of vaginal gel/ vaginal lubricant application