Safety and effectiveness of Alma plus laser device to reduce unwanted hair

Safety and effectiveness of Alma plus laser device (diode laser device) to reduce unwanted hair in the legs area.

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150101020514N19

Enrollment

Registered

2023-01-30

Start date

2023-04-09

Completion date

Unknown

Last updated

2023-02-07

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

Conditions

unwanted hair.

Interventions

Intervention group: 4 treatment sessions using Alma plus laser device produced by Sadra Aqua Company on right and left legs with wavelength at 808 nm, pulse width of 2 to 100 milli seconds and fluence

Eligibility

Sex/Gender

All

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Men and women aged 18 to 50 years Skin type 1-4 Signing the consent form for participation in the study

Exclusion criteria

Exclusion criteria: History of using any type of laser hair removal in the treatment area in the last 12 weeks If the percentage of white hair in the area is more than 5% Pregnancy or lactating

Design outcomes

Primary

Measure	Time frame
The rate of reduction of legs hairs in both sides. Timepoint: Before the intervention and 3 months after the last treatment session. Method of measurement: Trichoscopy By Fotofinder.	—

Secondary

Measure	Time frame
Comparison of pain level in both sides. Timepoint: Right after each treatment. Method of measurement: Visual analog scale (VAS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzin Ayatollahi

Tehran University of Medical Sciences

azinay@gmail.com+98 21 8897 7921

Outcome results

None listed

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