Comparison of suction blister and micro punch grafting methods in the treatment of patients with stable vitiligo

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210206050270N1

Enrollment

Registered

2021-07-21

Start date

2020-10-01

Completion date

Unknown

Last updated

2021-08-30

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: Intervention group: Punch graft 1) Sterilize the graft site 2) The site will be anesthetized with topical lidocaine.3) Harvesting 100-200 2 mm punches in one or more stages 4) Graft im

Eligibility

Sex/Gender

All

Age

13 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with persistent vitiligo are resistant to medical treatment, ie they have not had a new lesion in the past year and their previous lesions have not become larger. Patients should be between 13 and 65 years old Patients must give informed consent Patients should be willing to cooperate during the study and follow-up period.

Exclusion criteria

Exclusion criteria: Patients with immunodeficiency atients with bleeding disorders Patients being treated for other illnesses

Design outcomes

Primary

Measure	Time frame
Having Complaints. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire- visual analog scale (VAS).;Improvement Score. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire-visual analog scale (VAS).;Satisfaction Score. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire -visual analog scale (VAS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtefe Samimi

Esfahan University of Medical Sciences

atsamimi71@gmail.com+98 31 3782 0132

Outcome results

None listed

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