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A Clinical Study Evaluaing the Efficacy, Safety, and Patient Satisfaction of Injectable Hylaronic Acid With 0.3% Lidocain Hydrochloride, Prevelle Silk, for Superficial, Vertical Perioral Lines and Superficial, Horizontal, Lateral Canthal Lines

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2010 by Goldman, Butterwick, Fitzpatrick and Groff.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Mentor Worldwide, LLC
Information provided by:
Goldman, Butterwick, Fitzpatrick and Groff
ClinicalTrials.gov Identifier:
NCT01267149
First received: December 23, 2010
Last updated: December 27, 2010
Last verified: December 2010
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: No date given
  Estimated Primary Completion Date: No date given