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RecruitingAccepts healthy volunteersPhase 4

Evaluation of Filler Injection for Chin Profile Enhancement

University of Pennsylvania · NCT07777926

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 22–55 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 4
Target enrollment
20
US sites recruiting
1
Study start
September 30, 2026
Record last updated
August 20, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The goal of this prospective study is to analyze volumetric changes in the lower face after hyaluronic acid filler injections over 90 days.

The primary aim of the study is to quantify volume change of the lower face rea over time after injection of filler. The secondary aim is to collect patient related outcomes (PROs) via FACE-Q.

Participants will receive hyaluronic acid filler injections (Restylane Lyft(for contouring of the chin. Each patient will receive FDA approved dosages of filler to the lower face region to treat chin regression or chin contouring, as per FDA approved indications.

Prior to injections patients will be imaged with 3-dimensional photogrammetry. Subjects will return post-injection in 2 weeks, 1 month, and 3 moths for re-imaging.

Being studied: HA Filler

Conditions: Chin Regression; Chin Asymmetry; Jawline Contour Deficit

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Age 22-55
  • Patients interested in chin profile enhancement.
  • Participants must sign the informed consent form.

Exclusion Criteria

  • Prior filler for facial contouring
  • Filler injection within the past 12 months or during duration of study
  • Prior facial cosmetic surgery (i.e.. facelift)
  • Prior facial trauma (i.e.. orbital fracture)
  • Pregnant or breastfeeding at the time of injection (initial visit)
  • Planned dental work within next 2 weeks
  • The following contraindications: patients with known hypersensitivity or severe allergies manifested by a history of anaphylaxis or history or presence of multiple severe allergies, gram-positive bacterial protein allergies, lidocaine allergies or other local anesthetics of the amide type
  • Patients with known bleeding disorders

Recruiting US locations

Study contacts (from the official record)

  • Aamirah McCutchen · 215-360-0652 · aamirah.mccutchen@pennmedicine.upenn.edu
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Evaluation of Filler Injection for Chin Profile Enhancement (NCT07777926) | Bored Studies