Skip to content

Comparison study of effect of two concentrations of intra-lesional injection of a drug in patchy hair loss of the scalp

Comparison of therapeutic efficacy and safety of two concentrations of intra-lesional triamcinolone acetonide in patchy alopecia areata of the scalp: an open label randomized trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047692
Enrollment
44
Registered
2022-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: L639- Alopecia areata, unspecified

Interventions

Intervention1: Intralesional Triamcinolone Acetonide injection 5 mg/ml: Intra-lesional injection of triamcinolone acetonide in patch of alopecia areata (10mg/ml)
under aseptic conditions, using a 0.5 inch long, 30 gauge needle, fitted to an insulin syringe, a session every 3 weeks for 4 sessions or until complete hair re-growth whichever is earlier. The ste
under aseptic conditions, using a 0.5 inch long, 30 gauge needle, fitted to an insulin syringe, a session every 3 weeks for 4 sessions or until complete hair re-growth whichever is earlier. 0.1 ml

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of both sexes(males and females), aged >13 years with AA, 2. Patients having AA on the scalp with 3. Patients who had not taken any form of treatment in the last 8 weeks. 4. Patients who are willing to sign the written consent form before participating in the study

Exclusion criteria

Exclusion criteria: 1. Patients aged 2. Patients with alopecia totalis, alopecia universalis and ophiasis. 3. Patients having skin diseases affecting the scalp. 4. Patients with active infection at the local site and with keloidal tendency. 5. Pregnant or lactating women or immuno-compromised patients or patients with bleeding or coagulation disorders

Design outcomes

Primary

MeasureTime frame
Reduction in Severity Alopecia Tool (SALT) Score, 5 point semi-quantitative Re Growth Scale (RGS) and Dermoscopic AssessmentTimepoint: At Baseline,3 weeks, 6 weeks, 9 weeks,12 weeks

Secondary

MeasureTime frame
Assess side effects with two concentrations of intra-lesional injection of triamcinolone acetonideTimepoint: Every 3 weeks then at the 3 months of therapy from baseline (3weeks after the 4th session)

Countries

India

Contacts

Public ContactDr Bhavnish Bansal

All India Institute of Medical Sciences, Bathinda

drshivani.derm@gmail.com8287020404

Outcome results

None listed

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