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A prospective clinical study to compare efficacy and safety of 308 nm excimer laser and intralesional steroid injection for treatment of alopecia areata

Effectiveness and safety of 308 nm excimer laser versus intralesional triamcinolone acetonide for the treatment of alopecia areata; A randomized control trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071507
Enrollment
60
Registered
2024-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: L638- Other alopecia areata

Interventions

Intervention1: Intralesional steroid -triamcinolone acetonide(5mg /ml): Intralesional steroid ( triamcinolone acetonide 5 mg/ml ) given intradermally in small volumes of 0.1 ml once in 4 weeks on week

Sponsors

SRM Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients of 18 years of age and above attending SRM MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTER dermatology OPD, diagnosed with alopecia areata. 2. Patients having 1-5 patches on the scalp. 3. Patients who have not received any hair related treatment in the past 3 months 4. Patients providing voluntary informed and written consent for the explained treatment modality to be performed.

Exclusion criteria

Exclusion criteria: 1. Other types of AA such as ophiasis, sisapho, totalis , universalis 2. Patients with single alopecic patch greater than 6x6 sq.cm Total area of all patches combined should not exceed 80 sq.cm 3. Pregnancy or breastfeeding 4. Infection 5. Other immunological disorders and endocrine diseases which causes hair loss 6. Photosensitive skin 7. Patients unwilling to continue cooperation in the trial 8. Progressive AA during the trial

Design outcomes

Primary

MeasureTime frame
Extent and density of regrowth by the SALT scoring systemTimepoint: Week 0, 4 ,8 ,12 , 16 20 and 24

Secondary

MeasureTime frame
Global Aesthetic Improvement Scale, Patient satisfaction scoreTimepoint: Week 24;Visual Analogue ScaleTimepoint: Week 0, 4 ,8 ,12 , 16, 20 and 24

Countries

India

Contacts

Public ContactAllam Priyanka Reddy

SRM Medical College Hospital and Research Centre

leecutis@gmail.com9840168711

Outcome results

None listed

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