Estrogen and Platelet Rich Plasma in Treatment of Atrophic Vaginitis (NCT05118685) | Clinical Trial Compass
UnknownPhase 1
Estrogen and Platelet Rich Plasma in Treatment of Atrophic Vaginitis
Egypt100 participantsStarted 2021-11-13
Plain-language summary
This study is designed to compare the efficacy, acceptability, and safety of vaginal estrogen cream and platelet-rich plasma in pt. complaining of atrophic vaginitis.
Who can participate
Age range
50 Years – 70 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* postmenopausal women aged 50-70 years old
* with a clinical diagnosis of vaginal atrophy who will not need systemic estrogen therapy for the treatment of vasomotor symptoms or prophylaxis of osteoporosis
* Any parity.
Exclusion Criteria:
* Women with any history of carcinoma of the breast or endometrium,
* abnormal genital bleeding, acute thrombophlebitis, or thromboembolic disorders associated with previous estrogen use,
* or current urinary.
* In addition, women who underwent hormone replacement therapy, treated with systemic or vaginal estrogen within 6 months prior to the study,
* or had any contraindication for estrogen therapy will be excluded from the study.
Questions worth asking your doctor
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.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
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.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
improvement in Vaginal Health Index (VHI).
Timeframe: 12 weeks
2
improvement in Vulvovaginal atrophy (VVA) symptoms using the Visual analog scale (VAS).
Timeframe: 12 week
3
Assessment of quality of sexual function using the validated Portuguese version of the Female Sexual Function Index (FSFI)