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A Study Comparing Lafullen15 and Lafullen for Temporary Nasolabial Fold Improvement
Sponsor: Samyang Biopharmaceuticals Corporation
Summary
The objective of this clinical trial is to verify the safety and efficacy of Lafullen15 in the temporary improvement of nasolabial Folds
Official title: A Randomized, Evaluator-blind, Matched Pairs, Prospective, Non Inferiority, Confirmatory Study to Compare the Safety and Efficacy Between Lafullen15 and Lafullen in the Correction of Nasolabial Folds
Key Details
Gender
All
Age Range
19 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
73
Start Date
2024-05-27
Completion Date
2026-04-30
Last Updated
2024-05-14
Healthy Volunteers
No
Conditions
Interventions
Lafullen15
Apply a maximum of 1.0 ml for each side of the nasolabial fold using both the test device (Lafullen15) and the control device (Lafullen).
Lafullen
Apply a maximum of 1.0 ml for each side of the nasolabial fold using both the test device (Lafullen15) and the control device (Lafullen).