drugset / Trial / NCT01066026

Safety and Efficacy of a Metallic Cannula Versus A Standard Needle for Soft Tissue Augmentation of the Nasolabial Folds

NCT01066026

Phase 2 Completed 25 enrolled Hexsel Dermatology Clinic
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study was to assess the safety and efficacy of a new metallic cannula to inject hyaluronic acid for dermal augmentation in the nasolabial folds compared to standard needle.

Timeline

Start
2009-07
Primary completion
2010-01
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Background Hyaluronic Acid Other / unclassified 1 ml

Indications

No indication recorded.