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Early Intervention With Non-ablative Fractional Laser to Reduce Cutaneous Scarring

B

Bispebjerg Hospital

Status

Completed

Conditions

Cicatrix

Treatments

Device: non-ablative laser

Study type

Interventional

Funder types

Other

Identifiers

NCT02645773
Early intevention

Details and patient eligibility

About

To investigate intervention with early application of non-ablative laser to prevent scarring in the skin

Full description

To intervene in scar formation at three different time-points

Enrollment

16 patients

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • good health
  • men
  • Skin type 2-3
  • non-smokers
  • presenting full medical record

Exclusion criteria

  • active skin disease in test area
  • resent UV-exposure in test area
  • history of keloid
  • current or resent cancer
  • uncontrolled systemical disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

16 participants in 4 patient groups

Pre-laser
Experimental group
Description:
non-ablative laser Laser Pre-wounding low dose laser Pre-wounding medium dose laser Pre-wounding high dose
Treatment:
Device: non-ablative laser
Immediate-laser
Experimental group
Description:
non-ablative laser Laser low dose - immediate after wounding Laser medium dose - immediate after wounding Laser high dose - immediate after wounding
Treatment:
Device: non-ablative laser
Post-laser
Experimental group
Description:
non-ablative laser Laser low dose - post wounding Laser medium dose - post wounding Laser medium dose - post wounding
Treatment:
Device: non-ablative laser
Control
No Intervention group
Description:
Untreated control wound

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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