RecruitingPhase 2ACTRN12606000020583

Phyto-Soya Vaginal Gel Study

A randomized controll trial of Phyto-Soya Vaginal Gel for the relief of memopausal Vaginal Atrophy


Sponsor

Arkopharma Australia

Enrollment

60 participants

Start Date

Aug 1, 2005

Study Type

Interventional

Conditions


Eligibility

Sex: FemalesMin Age: 40 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing a vaginal gel containing phytoestrogens (plant-based oestrogen-like compounds from soy) for postmenopausal women experiencing vaginal dryness, itching, or painful sex. After menopause, falling oestrogen levels can cause the vaginal tissue to become dry and thin. This study tests whether this gel can relieve these symptoms as an alternative to hormonal treatments. You may be eligible if: - You are a postmenopausal woman aged 40 or older - You experience at least one of the following: vaginal dryness, vaginal itching, painful sexual intercourse, or elevated vaginal pH above 5 at screening You may NOT be eligible if: - You have used systemic or topical oestrogens within the past 8 weeks - You have used effective menopausal herbal remedies within the past 4 weeks - You have vulval dystrophy (a skin condition of the vulva) - You currently have a vaginal infection or urinary tract infection - You have had vaginal surgery in the past 12 months Talk to your doctor about whether this trial might be right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Intervention group would be women randomised into a group that will receive the Phy-Soya Vaginal Gel and

Intervention group would be women randomised into a group that will receive the Phy-Soya Vaginal Gel and


Locations(1)

Australia

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ACTRN12606000020583