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Microneedling vs Dermabrasion for Early Facial Scar Resurfacing

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Enrolling

Conditions

Scar

Treatments

Procedure: Dermabrasion
Procedure: Microneedling

Study type

Interventional

Funder types

Other

Identifiers

NCT06171386
IRB00102716

Details and patient eligibility

About

This study aims to determine whether microneedling or dermabrasion in the early post-operative period is superior in improving the appearance of surgical scars on the face.

Full description

Microneedling and dermabrasion are two common modalities that may be performed in-office to treat surgical scars.

Microneedling is a form of collagen induction therapy, often used in conjunction with platelet-rich plasma or hyaluronic acid.

Dermabrasion is a technique that improves the skin structure, quality, and appearance of scars through collagen remodeling and reepithelization.

To determine which modality is most effective, a prospective study; randomizing a volunteer sample of adult patients with new surgical vertical forehead scars will receive either dermabrasion or microneedling in the early postoperative period.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Volunteer adult patients will be identified by visiting the Facial Plastics and Reconstructive Surgery Clinic at Atrium Health Wake Forest Baptist.
  • Patients will be 18 years old+ and have a vertical surgical scar in the superior 1/3 of the face (trichion to glabella).
  • Patients will enroll in the clinic research registry and indicate an interest in being involved in the study.

Exclusion criteria

  • Patients who rate Types 4-6 on the Fitzpatrick scale will be excluded due to risk of poor outcome from dermabrasion.
  • There are no other planned exclusion criteria. Patients will not be excluded on the basis of gender, race/ethnicity, or age, provided that they meet the described inclusion criteria.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

microneedling
Active Comparator group
Description:
microneedling is a form of collagen induction therapy, often used in conjunction with platelet-rich plasma or hyaluronic acid - Patients will receive two treatments, once at 6-8 weeks following facial surgery, and the second at 12-16 weeks following facial surgery
Treatment:
Procedure: Microneedling
dermabrasion
Active Comparator group
Description:
dermabrasion is a technique that improves the skin structure, quality, and appearance of scars through collagen remodeling and reepithelization - Patients will receive the standard of care treatment 6-10 weeks following facial surgery
Treatment:
Procedure: Dermabrasion

Trial contacts and locations

1

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Central trial contact

Lauren G Himes, MD; Candace M Waters, MD

Data sourced from clinicaltrials.gov

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