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Evaluation of laser efficacy in treatment of cutaneous leishmaniasis lesion

Evaluation of fractional CO2 laser efficacy in treatment of atrophic scar of cutaneous leishmaniasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404303862N12
Enrollment
40
Registered
2014-07-03
Start date
2013-04-21
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

Cutaneous Leishmaniasis. Cutaneous Leishmaniasis

Interventions

Cleansing of location by isopropyl alcohol 70%, and then dressing is performed for local anesthesia. After 45 minutes, the location is washed and dried. Treatment will be performed with laser beam siz
Treatment - Devices

Sponsors

Mashhad University of Medical Sciences, Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age more than 12 years old; informed consent of patient for participating in study; atrophic scar in hand or face with duration of improvement more than one year Exclusion criteria: patients with chronic disease like diabetes and collagen vascular diseases that have a problem in scar healing; hypertrophic or keloid scars; history for receiving isotretinoin during last year; pregnancy or breastfeeding; immunodeficiency patients like patients under immunosuppressive medicines; patients who don’t complete treatment period or don’t refer for follow ups; skin type VI; history of radiotherapy in laser locations; patients with positive coiner disease like psoriasis and vitiligo

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Complete healing. Timepoint: For the first before intervention, then during therapy sessions, and 3 and 6 months after the last treatment session. Method of measurement: Measuring the size of induration and scar.

Secondary

MeasureTime frame
Side effects including erythema, edema, petechiae, dispigmentation and scar. Timepoint: start of therapy, 3 and 6 months after the last treatment session. Method of measurement: Physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hamid Reza Moghimi

Mashhad University of Medical Sciences

src@mums.ac.ir+98 51 1841 0135

Outcome results

None listed

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