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Evaluating the safety and effectiveness of Prime eyelash strengthening serum

Evaluating the safety and effectiveness of Prime eyelash strengthening serum in improving hypotrichosis of eyelashes and increasing their length and thickness

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190210042676N34
Enrollment
20
Registered
2024-09-05
Start date
2024-09-22
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Hypotrichosis of eyelashes.

Interventions

Intervention group: 12 weeks of using Prime eyelash strengthening serum produced by Akhavi laboratory contains deionized water, Butyl glycol, Dextran, Acetyl tetrapeptide-3, red clover flower extract,

Sponsors

Akhavi laboratory
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 18 -65 years old men and women Idiopathic eyelash hypotrichosis with grade 1 or 2 (with Global Eyelash Assessment (GEA) criteria) Signing the informed consent form

Exclusion criteria

Exclusion criteria: Suffering from uncontrolled systemic diseases or any type of disease or condition (chemotherapy,...) that causes abnormality in hair of ??eyelashes, eyebrows or head area. History of known eye diseases (except for refractive errors) such as high intraocular pressure, corneal inflammation, degenerative eye diseases, cataracts, glaucoma, etc. History of eye surgeries in the last 3 months Eyelash extensions or transplant in the last three months Pregnancy and lactating

Design outcomes

Primary

MeasureTime frame
Percentage of people with one grade or more improvement in GEA scale. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Scoring eyelash thickness using digital photos based on Allergan Global Eyebrow assessment (GEA).

Secondary

MeasureTime frame
Patient satisfaction from treatment. Timepoint: Before intervention, 6 and 12 weeks after intervention. Method of measurement: Using a 4-point Likert scale.;Comparison of upper eyelash hair thickness. Timepoint: Before intervention, 6 and 12 weeks after intervention. Method of measurement: Trichoscan.

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