Efficacy and Safety of Topical Vitamin D Analogue in Treatment of Female Pattern Hair Loss (NCT06333600) | Clinical Trial Compass
UnknownPhase 1/2
Efficacy and Safety of Topical Vitamin D Analogue in Treatment of Female Pattern Hair Loss
Egypt45 participantsStarted 2023-05-20
Plain-language summary
The trial aims to study efficay of topical vitamin D analogue in treatment of female pattern hair loss cases
Who can participate
Age range
15 Years – 60 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:
* All females with FPHL aging 15 - 60 years
Exclusion Criteria:
* Patients with other hair loss disorders as telogen effluvium, anagen effluvium, alopecia areata, cicatricial alopecia and trichotillomania.
* Patients with normal serum vit.D level
* Oral or parentral vitamin D supplementation for the last 3 months
* Treatment with topical vitamin D analogs in the past month
* Patients who received hair tonics or any specific hair therapy over the last 3 months prior to enrollement in the study.
* Patients with diabetes mellitus, renal disease, thyroid and parathyroid abnormalities, or autoimmune diseases.
* Patients who are pregnant, lactating or on contraceptive pills.
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
Change of Sinclaire grading of Female pattern hair loss
Timeframe: 3 months
2
Change of Trichoscopic parameters (Hair dermoscopy)