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Evaluation of safety and the effectiveness of Caffeine Plus Irox anti-hair loss serum and shampoo

Evaluation of safety and the effectiveness of Caffeine Plus Irox anti-hair loss line (serum and shampoo) produced by Iran Avandfar company In the prevention and treatment of androgenic hair loss

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190210042676N13
Enrollment
20
Registered
2021-05-08
Start date
2021-05-15
Completion date
Unknown
Last updated
2021-05-26

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: Topical use of Caffeine Plus Irox anti-hair loss serum produced by Iran Avandfar company(Contains Canadian willow extract, Glycolic extract of green tea, Caffeine , etc..)20 drops

Sponsors

Iran Avandfar Company
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Male aged 18-55 years Good general health Voluntary participation and sign the written informed consent Hair Loss Status II, III, IV based on Norwood Scale

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 People with allergies to serum and shampoo ingredients Any severe weight loss or strict diet therapy during the study

Design outcomes

Primary

MeasureTime frame
Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 6 and 12 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 .

Secondary

MeasureTime frame
Hair count changes. Timepoint: Before intervention, 6 and 12 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder.;Changes in percentage of anagen to telogen. Timepoint: Before intervention, 6 and 12 weeks the start of use. Method of measurement: Trichoscopy By Fotofinder.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAniseh Samadi

Tehran University of Medical Sciences

aniseh_samadi@yahoo.com+98 21 8896 0880

Outcome results

None listed

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