Jaw filler study tracks volume changes in 14 adults
NCT ID NCT06694857
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how hyaluronic acid filler (Juvéderm Volux XC) changes jaw volume over 90 days. Fourteen adults received FDA-approved doses for jaw contouring. Researchers used 3D imaging before injection and at 2 weeks, 1 month, and 3 months after to measure volume changes and patient satisfaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hyaluronic acid filler (Juvéderm Volux XC)
- What this could lead to
- If successful, this could help doctors predict how long jaw filler results last and improve patient satisfaction with contouring.
- What could go wrong
- This is a small, completed Phase 4 study with only 14 participants. Results may not apply to everyone, and filler effects vary by individual.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
14 people
The number who actually took part.
- Started
-
Oct 2024
- Finished
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Nov 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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22 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 22-55 2. Patients interested in jaw contouring 3. Participants must sign the informed consent form. Exclusion Criteria: 1Prior filler for facial contouring 2) Filler injection within the past 12 months or during duration of study 3) Prior facial cosmetic surgery (ie. facelift) 4) Prior facial trauma (ie. orbital fracture) 5) Pregnant or breastfeeding 6) Planned dental work within next 2 weeks 7) The following contraindications: patients with severe allergies manifested by a history of anaphylaxis or history or presence of multiple severe allergies, gram-positive bacterial protein allergies and lidocaine allergies
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Penn Medicine
Philadelphia, Pennsylvania, 19104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.