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Study on the safety and effectiveness of diode laser treatment for underarm hair reduction in adult Indian women

Safety and efficacy of Diode Laser for axillary hair reduction in adult Indian women A hospital-based observational study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/09/094765
Enrollment
20
Registered
2025-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: L688- Other hypertrichosis

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Sanjana Yadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult females (more than 18 years of age) patients presenting to the Dermatology OPD with unwanted axillary hair, willing for laser hair reduction. Willing to undergo multiple treatment sessions and follow-up assessments. Patients who give informed consent for the study and photography.

Exclusion criteria

Exclusion criteria: Patients with photo-aggravated skin diseases and medical illness, e.g., systemic lupus erythematosus (SLE) Presence of active cutaneous infections or dermatoses in the treatment area, e.g., dermatophytosis, Staphylococcal infections, psoriasis etc. Keloidal tendency. Pregnant or lactating women. Patients who have previously undergone laser treatment in axilla.

Design outcomes

Primary

MeasureTime frame
To assess the safety and efficacy associated with Vacuum-Assisted Laser delivery system. Timepoint: Baseline and after every visit, approximately 4 week intervals for minimum of 4 and maximum of 8 sessions

Secondary

MeasureTime frame
To assess the safety and efficacy of Vacuum assisted laser and 9x9mm Chill tip diode laser. To assess patient satisfaction with each modality. To compare Pre and Post treatment Hair Count and Texture using Dermoscopy and Photographs with novel Gabor Filter software. To compare manual hair counts with AI/Software-based assessments in evaluating treatment outcomes. Timepoint: Baseline and after every visit, approximately 4 week interval

Countries

India

Contacts

Public ContactDr Varsha Shetty

Kasturba Medical College, Manipal Academy of Higher Education

varshams18@gmail.com9902394514

Outcome results

None listed

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