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A study to compare the effect of whole body NB-UVB (phototherapy) versus targeted NB-UVB ( hand and foot phototherapy) in re-pigmentation of acral (hand and feet) vitiligo

A RANDOMISED SPLIT BODY COMPARATIVE TRIAL TO STUDY THE EFFECT OF WHOLE BODY NB-UVB VERSUS TARGETED NB-UVB ON STABILITY AND RE-PIGMENTATION OF ACRAL VITILIGO

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/037998
Enrollment
30
Registered
2021-11-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: Whole body NB-UVB therapy to whole body except for hand/feet covered with gloves: NB-UVB will be administered thrice weekly on alternate days. The starting dose will be on 200mJ/cm2or 7

Sponsors

PGIMER Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of non-segmental vitiligo with body surface area involved 10-50%. 2. Bilateral lesions over the acral parts (lesions on hands/feet). 3. Active disease defined by VIDA 4+, occurrence of new lesions, progression of existing lesions, Koebnerisation. 4. Age 12-60 years

Exclusion criteria

Exclusion criteria: 1. Patients of segmental Vitiligo. 2. History of previous phototherapy or other immunosuppressive treatment. (â??For patients using any local or systemic immunosuppressive therapy, a washout period of 8 weeks is requiredâ??). 3. Patients without acral lesions. 4. Contraindications to use of NB-UVB 5. Intake of phototoxic drugs 6. History of skin malignancy or any current pre-malignant condition. 7. Claustrophobia 8. Hepatic or renal dysfunction

Design outcomes

Primary

MeasureTime frame
1.Proportion of patients achieving VIDA 3+ from baseline VIDA score of 4+ in both groups at 12 weeks follow-up 2.Proportion of patients achieving 50% improvement from baseline limb specific VASI in both groups at 24 weeks of follow-up Timepoint: 4weekly for 24 weeks

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactAnish Thind

PGIMER, Chandigarh

vinay.keshavmurthy@gmail.com8872993222

Outcome results

None listed

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