Prospective Evaluation of Facial Cosmetic Procedures
| Status: | Not yet recruiting |
|---|---|
| Healthy: | No |
| Age Range: | 40 - 65 |
| Updated: | 2/24/2019 |
| Start Date: | April 15, 2019 |
| End Date: | March 1, 2020 |
| Contact: | Robyn Broach, PhD |
| Email: | robyn.broach@uphs.upenn.edu |
| Phone: | 215-360-0640 |
Prospective Evaluation of Minimally Invasive Facial Cosmetic Procedures Through Measured Volumetric Changes and Patient Reported Outcomes
A prospective, trial to quantitatively and qualitatively compare the dermal fillers for the
treatment of age related aesthetic changes.
treatment of age related aesthetic changes.
Dermal fillers have been approved for the treatment of age related aesthetic changes,
including facial volume loss, and attenuation of the static and dynamic rhytid. Despite
widespread use of volumizing fillers there is little data quantifying the subjective benefit
of these minimally invasive treatments from the patient perspective. Furthermore, there is
little data comparing the subjective benefit with true objective volumetric results. Such
data will provide much needed information for patient counselling and treatment optimization
for patient perceived outcomes.
This study is to determine the patient reported outcomes of three different dermal fillers
and establish the volumetric changes over 90 days. Screening will be performed during the
patient's office visit. Approximately 100 patients will be enrolled. Patients will
participate up to 90 days (Day 1, 14 days, 28 days, and 90 days).
including facial volume loss, and attenuation of the static and dynamic rhytid. Despite
widespread use of volumizing fillers there is little data quantifying the subjective benefit
of these minimally invasive treatments from the patient perspective. Furthermore, there is
little data comparing the subjective benefit with true objective volumetric results. Such
data will provide much needed information for patient counselling and treatment optimization
for patient perceived outcomes.
This study is to determine the patient reported outcomes of three different dermal fillers
and establish the volumetric changes over 90 days. Screening will be performed during the
patient's office visit. Approximately 100 patients will be enrolled. Patients will
participate up to 90 days (Day 1, 14 days, 28 days, and 90 days).
Inclusion Criteria:
- Female patients 40 - 65 years of age
Exclusion Criteria:
- Male patients
- Prior surgical facial rejuvenation procedures
- Facelift
- Neck lift
- Blepharoplasty
- Facial fat grafting
- Prior minimally invasive rejuvenation procedure ≤ 12 months
- Known contraindications to devices or drugs used in this study
- Facial paralysis
- Congenital facial asymmetry
- Pregnant women
- Patient actively taking blood thinners
We found this trial at
1
site
Philadelphia, Pennsylvania 19104
Principal Investigator: Ivona Percec, MD, PhD
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