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Study of effectiveness of Topical 10% Potassium Hydroxide In Treatment Of Localized Vitiligo

The Experimental Study Of Effectiveness Of Topical 10% KOH As The Treatment Of Localized Vitiligo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026235
Enrollment
84
Registered
2020-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L80- Vitiligo

Interventions

Intervention1: 10% KOH: Apply topically 10% KOH to localized lesions of Vitiligo for 15 min every 2 weeks for 12 weeks. Control Intervention1: Not Applicable: Not Applicable

Sponsors

MGM Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients Having Localized vitiligo lesions 2.Patients Having Segmental vitiligo lesions 3.Patients willing for treatment and follow up

Exclusion criteria

Exclusion criteria: 1.Facial vitiligo 2.Pregnancy and lactation. 3.Keloid 4.Recent herpes infection.

Design outcomes

Primary

MeasureTime frame
To study the effectiveness of topical 10% KOH in treatment of Localized Vitiligo.Timepoint: Every 2weeks for 12weeks—

Secondary

MeasureTime frame
To study the adverse effects of topical 10% KOH in treatment of Localized Vitiligo.Timepoint: Every 2weeks for 12weeks—

Countries

India

Contacts

Public ContactDr Saujanya Sagar

MGM Medical College And Hospital Aurangabad

ashish7557@gmail.com9422213292

Outcome results

None listed

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