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Evaluation of safety and efficacy of Revola Chang mesotherapy product in reducing hair loss

Evaluation of safety and efficacy of Revola Chang mesotherapy product in reducing diffuse and scattered hair loss and improving hair volume and density

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190210042676N42
Enrollment
20
Registered
2025-02-23
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-07-21

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: Three sessions of injection of Revola Chang mesotherapy solution made by Novajen Daru CO. (1.5 ml per session) with an interval of 2 weeks on the entire scalp. Ingredients: Sodium

Sponsors

Novajen Daru
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Male or female aged 18-55 years Diffuse and scattered hair loss (Count at least 300 hairs in a combing test over three days) General health Voluntary participation and signing written informed consent

Exclusion criteria

Exclusion criteria: Men and women with androgenetic pattern hair loss (Hamilton grade 3 and above in men and Ludwig grade 2 and above in women) Pregnancy or breastfeeding Clinical hyperandrogenism in the form of pronounced hirsutism and menstrual disorders in women Chronic active scalp disease other than hair loss Using any prescribed drug or Over The Counter(OTC) for hair loss within the past 3 months

Design outcomes

Primary

MeasureTime frame
Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 6 and 12 weeks after the intervention. 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, 8 and 12 weeks after the intervention. Method of measurement: Trichoscopy by Fotofinder.;Terminal hairs count. Timepoint: Before intervention, 8 and 12 weeks after the intervention. 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