A retrospective study to evaluate the Ulthera® System for its potential interaction with toxins and fillers. Up to 500 subjects will be enrolled.
This is a retrospective, multi-site study involving chart reviews of subjects who have received an Ultherapy treatment along with Radiesse®, Xeomin®, and/or Belotero® Balance within six months apart in the face and/or neck areas. Enrolled subjects will have received an Ultherapy treatment along with botulinum toxin A and/or filler treatment(s) within the last two years and with filler and toxin treatment occurring within 6 months before or after Ultherapy.
Study Type
OBSERVATIONAL
Enrollment
101
Focused ultrasound energy delivered below the surface of the skin.
An injectable medicine used to temporarily improve the look of moderate to severe frown lines between the eyebrows (glabellar lines) in adults.
An injectable dermal filler that temporarily adds volume to help smooth moderate to severe facial wrinkles and folds, such as nasolabial folds (the creases that extend from the corner of the nose to the corner of the mouth).
Aesthetic Plastic Surgical Institute
Laguna Beach, California, United States
Dermatology Cosmetic Laser Medical Associates of La Jolla
San Diego, California, United States
Skin Research Institute
Coral Gables, Florida, United States
Maryland Laser Skin and Vein Institute
Hunt Valley, Maryland, United States
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
An assessment of adverse events through chart review will evaluate the safety of combination treatments of Ultherapy with toxins/fillers.
Time frame: Within 6 months before or after Ultherapy
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An injectable dermal filler to temporarily smooth out and fill in moderate-to-severe nasolabial folds (the folds or wrinkles that go from the side of the nose to the corner of the mouth).
Premier Clinical Research
Spokane, Washington, United States