Intense Pulsed Llight in treatment of Nevus Spilus in patients attending dermatology clinic of razi hospital

Intense Pulsed Light in Treatment of Nevus Spilus in in patients attending dermatology clinic of razi hospital

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014052414285N2

Enrollment

Registered

2014-07-09

Start date

2013-06-01

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Nevus Spilus. Melanocytic naevi

Interventions

Included patients will be treated by Intense pulsed light system with these parameters: pulse width 10-30ms, Fluence 44-50 jouls. treatment will be conducted for three consecutive sessions one month t

Treatment - Devices

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: inclusion criteria : nevus Spilus confirmed via histopathology Exclusion Criteria : pregnancy; lactation; tanning, scar formation history; previous treatment with laser

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Decrease in Color Density. Timepoint: one months. Method of measurement: Photography Comapring.	—

Secondary

Measure	Time frame
Ulceration. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.;Hypopigmentation. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.;Scar formation. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.	—

Measure

Time frame

Ulceration. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.;Hypopigmentation. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.;Scar formation. Timepoint: Beggining of the study, First Month, Second Month, Third Month, at the end of the study. Method of measurement: Clinical Exam.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Hooshang Ehsani

Razi Hospital

ehsanih@sina.tums.ac.ir+98 21 5561 8989

Outcome results

None listed

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