Study of the efficacy of nano dressing in comparison common dressing treatment of vitiligo

Study of the efficacy of nano dressing in comparison common dressing after grafting of epidermal suspension containing melanocyte and keratinocyte in treatment of resistant vitiligo

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130812014333N133

Enrollment

130

Registered

2019-12-25

Start date

2020-01-10

Completion date

Unknown

Last updated

2020-01-13

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

Conditions

Vitiligo. Vitiligo

Interventions

Intervention 1: The intervention group will be dressed for one week with biodegradable and biodegradable nano dressing prepared by electrospinning. Intervention 2: The control group will be dressed wi

Eligibility

Sex/Gender

All

Age

11 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 11 and 60 Patients with vitiligo who have not been treated with corticosteroids or PUVA for at least 12 weeks No active vitiligo The absence of the Kubner phenomenon in the past

Exclusion criteria

Exclusion criteria: Fertile and lactating women Colloid history

Design outcomes

Primary

Measure	Time frame
Wound healing. Timepoint: The first month is weekly and then monthly for up to 6 months. Method of measurement: Medical Imaging.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Eftekharipour

Kermanshah University of Medical Sciences

Hamideftekharipirous@gmail.com+98 83 3835 9054

Outcome results

None listed

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