Skip to content

The effectiveness of Combination 3D diode laser hair removal device

The effectiveness of Combination 3D diode laser hair removal device

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240612062105N1
Enrollment
60
Registered
2024-08-12
Start date
2024-06-20
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Hypertrichosis. Hypertrichosis

Interventions

Intervention 1: Intervention group: 30 patients seeking hair removal who, after being examined by a specialist doctor and meeting the eligibility criteria, will receive this treatment (hair removal wi

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion: 60 participants over 18 years of age seeking hair removal, including 30 with the combined 3D diode device and 30 with the conventional device (CYNOSURE Apogee Elite Plus, which is an alexandrite laser), participated in this study.

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding Any severe medical condition Consumer disorders Dermatitis Pigmentery disorder Proven tumors History of laser hair removal Presence of photo-exacerbated disease Evidence of skin infection Use of any systemic retinoids in the past 6 months Impairment of the immune system or the use of immune system inhibitors Simultaneous treatment with hair reduction drugs The presence of background hormonal disorders History of sun exposure History of keloid formation in the body

Design outcomes

Primary

MeasureTime frame
The reduction in hair is assessed by evaluators based on the following percentages: less than 25%, 25% to 50%, 50% to 75%, and more than 75%. Timepoint: Each participant undergoes six laser treatment sessions at intervals of 4 to 8 weeks. Before each session and one month after the last session, images of a specific anatomical area of the patient are taken with a digital camera. These images are then assessed blindly by three expert evaluators, who have had no involvement in the study, and the percentage of hair reduction is reported. Method of measurement: Each participant undergoes six laser treatment sessions at intervals of 4 to 8 weeks. Before each session and one month after the last session, images of a specific anatomical area of the patient are taken with a digital camera. These images are then assessed blindly by three expert evaluators, who have had no involvement in the study, and the percentage of hair reduction is reported.

Secondary

MeasureTime frame
Patients express their satisfaction based on a 4-point scale: hair reduction of less than 25%, 25% to 50%, 50% to 75%, and greater than 75%. Timepoint: Before each treatment session. Method of measurement: Based on a 4-point scale: hair reduction of less than 25%, 25% to 50%, 50% to 75%, and greater than 75%.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsima davoodi

Mashhad University of Medical Sciences

davoudis@mums.ac.ir0098516041695

Outcome results

None listed

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