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Pulsed Dye Laser Treatment of Recent Surgical Scars

G

Ghent University Hospital (UZ)

Status

Completed

Conditions

Surgical Scars

Treatments

Procedure: Pulsed dye laser treatment
Procedure: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT01201525
2009/218

Details and patient eligibility

About

Hypothesis: Improvement of recent surgical scars after treatment with 595nm Pulsed dye laser treatments.

Study design: Prospective single blinded within patient controlled randomised trial. Recent surgical scars of at least 5cm will be divided into 2 parts and randomized. 1 part will be treated with 4 595nm Pulsed dye laser treatments on a 4 weeks interval. The other part will serve as a within patient control. 1 and 6 months after the intervention both parts of the scar will be evaluated.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with planned surgical intervention leaving a scar from at least 5 cm in an area prone to hypertrophic scarring : neck, shoulders, chest, mandibular angle and extremities
  • Age at least 18 years old.
  • Patient able and willing to give written informed consent

Exclusion criteria

  • Patients with planned surgical intervention on hands, feet and genital area
  • Patients with a history of photodermatoses
  • Patients with a history of keloids
  • Patients with a history of adverse outcomes related to PDL

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups, including a placebo group

Surgical scar - part 1
Experimental group
Description:
Surgical scar - part 1
Treatment:
Procedure: Pulsed dye laser treatment
Surgical scar - part 2
Placebo Comparator group
Description:
Surgical scar - part 2
Treatment:
Procedure: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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