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 range15 Years – 60 Years
SexFEMALE
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.
What they're measuring
1
Change of Sinclaire grading of Female pattern hair loss
Timeframe: 3 months
2
Change of Trichoscopic parameters (Hair dermoscopy)