Clinical investigation of the safety and effectiveness of Excilia Hair strengthening and ani hair loss Lotion in improving hair loss

Clinical investigation of the safety and effectiveness of Excilia Hair strengthening and ani hair loss Lotion in improving male pattern androgenic hair loss

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210130050179N6

Enrollment

Registered

2023-02-12

Start date

2023-02-20

Completion date

Unknown

Last updated

2023-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hair loss. Nonscarring hair loss, unspecified

Interventions

Intervention group: Topically use of Excilia Hair strengthening and anti-hair loss lotion

Includes: Minoxidil oxathiazolidine carboxylate 5%, glycolic acid (AHA), caffeine, etc. for 24 weeks..

Eligibility

Sex/Gender

Male

Age

18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Male aged 18-55 years General health Hair Loss Status II, III, IV Based on Norwood Scale Voluntary participation and signing written informed consent

Exclusion criteria

Exclusion criteria: Chronic active scalp disease other than hair loss Using any prescribed drug or OTC for hair loss within the past 3 months Documented sensitivity to formulation components Any severe weight loss or strict diet therapy during the study Oral or topical treatment of minoxidil within 6 months before entering the study.

Design outcomes

Primary

Measure	Time frame
Count changes in terminal hair. Timepoint: Before intervention, 8,16,24 and 32 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder device.	—

Secondary

Measure	Time frame
Hair count changes. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder device.;Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: One independent dermatologist will perform clinical assessments in a blinded fashion by scoring every photograph according to the "Global photographic review" scale.	—

Measure

Time frame

Hair count changes. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder device.;Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: One independent dermatologist will perform clinical assessments in a blinded fashion by scoring every photograph according to the "Global photographic review" scale.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTaraneh Yazdanparast

Tehran University of Medical Sciences

drtaraneh@yahoo.com+98 21 8897 2220

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026