TrialReader


LONG PULSED ND:YAG LASER (1064 NM) VERSUS INTENSE PULSED LIGHT IN TREATMENT OF TRAUMATIC AND POST-SURGICAL ERYTHEMATOUS SCARS

NCT07599709 — Not applicable, Completed, 40 participants, Alexandria University

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  
RegistryNCT07599709
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, treatment
Enrollment40 (Actual)
SponsorAlexandria University (Other)
ConditionsScars
InterventionsLong pulsed ND: YAG laser, Intense Pulsed Light (Device)
Datesstart 2022-11-16, primary completion 2024-12-25, completion 2025-04-12, first posted 2026-05-20, last updated 2026-05-20
Locations1 site in Egypt

Related Papers Related Patents Related Grants Related Experts
AI Assistant Save
All trials for Scars All trials of Long pulsed ND: YAG laser All trials of Intense Pulsed Light

-Summary

The goal of this clinical trial is to compare the efficacy and safety of long-pulsed ND:YAG laser and intense pulsed light in the treatment of traumatic and post-surgical erythematous scars. Forty patients presenting with traumatic and post-surgical erythematous scars on the head and neck, of six months' duration or less, were randomly divided into two equal groups. Group A patients received long-pulsed ND:YAG laser sessions, while Group B patients received intense pulsed light sessions. Four sessions were given at four-week intervals.

Expand all sections  ·  Collapse all

+Arms and interventions

ArmTypeInterventionsDescription
Group AActive comparatorDevice: Long pulsed ND: YAG laser
Group BActive comparatorDevice: Intense Pulsed Light
  • Long pulsed ND: YAG laser (Device): Long Pulsed ND:YAG laser (1064 nm)
  • Intense Pulsed Light (Device): Intense Pulsed Light (light based modality)

+Outcome measures

Primary outcomes

  • Compare the efficacy and safety of long-pulsed Nd-YAG laser and intense pulsed light in the treatment of traumatic and post-surgical erythematous scars. [From enrollment to 3 months after last treatment sessions, where four sessions were given at four-week intervals.]: The efficacy were assessed using the Patient and Observer scar assessment scale as well as subjective and objective assessment of scar erythema

+Eligibility

Sex: All, ages: 12 Years to any

Inclusion Criteria:

Patients of either gender, aged more than 12 years, presenting with an erythematous scar on the head and neck area, traumatic or post-surgical, and of a duration equal to or less than six months.

Exclusion Criteria:

* 1\. Patients with post burn scars, scars of more than six months duration, keloids, post acne atrophic erythematous scars or scars that are not located on the head and neck area.

  2\. Patients with active bacterial, viral, or fungal cutaneous infection within the scar tissue.

  3\. Patients who are pregnant or lactating. 4. Known contraindication to laser therapy. 5. Use of Isotretinoin within the previous 6 months.

+Locations (1)

FacilityCityCountryStatus
Alexandria main university hospital, Department of dermatology and venerology.Alexandria, Alexandria GovernorateEgypt

My Notes