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In this study we will compare the combined role of medical treatment and surgical treatment in the management of vitiligo .

Evaluation of the role of immunomodulators in combination with Non-cultured epidermal cell suspension in the management of vitiligo- A quasi randomised controlled clinical trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/076098
Enrollment
56
Registered
2024-10-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: L80- Vitiligo

Interventions

Intervention1: IMMUNOMODULATORS WITH NON-CULTURED EPIDERMAL CELL SUSPENSION: After proper history and clinical examination , patients with more than 3 months of patch stability (denovo/induced stabili

Sponsors

AIIMS JODHPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) More than 3 months of patch stability (spontaneous or therapy induced) 2) Subjects with non-segmental /segmental vitiligo 3) Age =15 years

Exclusion criteria

Exclusion criteria: 1. Unstable for last 3 months 2. Universal vitiligo or exclusive involvement of tip of finger, toes or palmo plantar or genitalia 3. Vitiligo Patch size more than 100 cm2size 4. Pregnancy or lactation 5. Patients with bleeding diathesis or keloidal tendencies 6. Any known hypersensitivities or contraindication to immunomodulators or local anesthesia 7. Presence of any of the following : Immunocompromised patient, malignancy, co-morbidities like uncontrolled diabetes, chronic renal disease, chronic kidney disease

Design outcomes

Primary

MeasureTime frame
1)Repigmentation: a. Objective – Investigator global assessment (IGA) Vitiligo area severity index (VASI), Colour match, pattern of repigmentation, Dermoscopic assessment (BPLeFoSK criteria) b. Subjective - Patient global assessment (PGA) 2)Investigator Global Assessment (IGA) Patient Global Assessment (PGA) Timepoint: At baseline, 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks and 24 weeks.

Secondary

MeasureTime frame
1 Side effects will be noted 2 VIS-22 score assessment for quality of life Timepoint: At Baseline,4 weeks,8 weeks,12 weeks,16 weeks,20 weeks,24 weeks

Countries

India

Contacts

Public ContactDr Sabyasachi Debata

AIIMS JODHPUR

saurabhdoc@yahoo.co.in9968024250

Outcome results

None listed

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