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Starting soon Not applicable

Effect of Minoxidil Solution Iontophoresis on Androgenic Alopecia

NCT07056933 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-07-08
Last updated
2025-07-09

Condition(s) studied

Alopecia

Investigational drug(s) / intervention(s)

Minoxidil solution iontophoresissaline solution iontophoresis

Minoxidil solution iontophoresis: The half of the scalp of the participants will be treated with 5% minoxidil solution through Iontophoresis that will be applied at small low voltage (typically 10 V or less) continuous constant current (typically 0.5 mA/cm2 or less) to push a charged drug into skin or other tissue, twice daily at home.

saline solution iontophoresis: The other half of the scalp of the participants will be treated with placebo saline solution ( control) with the current application.

Study summary

The aim of the study is to evaluate the therapeutic efficiency of minoxidil solution iontophoresis on Androgenic Alopecia.

Eligibility

Sex
MALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Twenty-five adult aged 18-65 with diagnosed androgenic alopecia. * They diagnosed as Androgenic alopeacia by their physicians and referred for physical therapy management. * Medically and psychologically stable patients. Exclusion Criteria: * History of hypersensitivity to minoxidil solution or Intophoresis. * Scalp infection * Concurrent hair loss treatments. * Patients who suffer from hypertrophic and/or keloidal scars and a skin condition in the area of Androgenic alopecia that would interfere with study procedures. * plaque psoriasis, tattoo, birthmark, facial hair. * Patients with medical red flags as severe psychiatric disorder or cognitive deficits. * Medically unstable and uncooperative patients. * Immunocompromised status. * History of skin cancer. * Recurrent herpes viral infection. * Pregnancy or breastfeeding status.

Primary outcome measure(s)

  • Change in the number of hair follicles — 12 weeks
    Trichoscopy will be used to detect the change in the number of hair follicles as a comparison between before and after intervention. Trichoscopy helped with the definitive diagnosis of Alopeacia in patients for whom the clinical diagnosis was doubtful, which was confirmed by histopathology. Thus trichoscopy is a noninvasive, sensitive and specific investigation that is valuable in women with alopecia, the cause of which is otherwise very difficult to assess clinically, and it has a definite role in the diagnosis of cases with an atypical clinical picture.Trichoscopy results were obtained in frontal, occipital and both temporal areas of scalp, including number of yellow dots and vellus hairs, number of hairs in one pilosebaceous unit and percentage of follicular ostia with perifollicular hyperpigmentation.

Trial sites (1)

FacilityCityRegionStatus
Mahmoud Ibrahim Mohamed Zagazig Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07056933 on ClinicalTrials.gov ↗ ← All trials in Egypt