Safety and Effectiveness of Aquamid as Compared to Restylane for the Aesthetic Treatment of Nasolabial Folds
Completed · Not applicable
Conditions studied: Facial Wrinkles
In brief
The purpose of this study is to compare the effectiveness of Aquamid and Restylane in aesthetically enhancing nasolabial folds 6 months after treatment and to evaluate the safety of Aquamid through 12 months after treatment. The study includes an extended follow up to 24 months.
Key facts
- Study ID
- NCT00407914
- Run by
- Contura
- People needed
- 315
- Starts
- 2006-12-01
- Expected to finish
- 2009-07-01
- Last updated by the study team
- 2009-10-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- interested on soft tissue augmentation for the nasolabial folds
- moderate to severe nasolabial fold
You may not qualify if…
- sensitivity to anesthetics
- allergy to hyaluronic acid
- previous treatment with permanent fillers in the treated area
- recent previous aesthetic procedure in the treatment area
- infected skin areas or autoimmune diseases affecting the skin
Where it is running
- Study site — White Plains, New York, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.