Clinical Trials Directory

Trials / Completed

CompletedNCT06372782

Comparing Pain, Safety and Effectiveness of Restylane Skinboosters Vital Lido and Vital Without Lido in Dorsal Hand

A Randomized, Split-Hand, Subject-Blinded Study Comparing Pain, Safety and Effectiveness of Restylane Skinboosters Vital Lidocaine and Restylane Vital Without Lidocaine for Improved Appearance of the Dorsal Hand in Chinese Subjects

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Galderma R&D · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a randomized, multi-center, split-hand, subject-blinded study comparing pain, safety and effectiveness of Restylane Skinboosters Vital Lidocaine and Restylane Vital without lidocaine for improving appearance of the dorsal hands in Chinese subjects.

Conditions

Interventions

TypeNameDescription
DEVICERestylane Skinboosters Vital LidocaineEach subject will receive treatment on Day 1 with Restylane Skinboosters Vital Lidocaine in one hand and Restylane Vital in the opposite hand, as randomly assigned.
DEVICERestylane VitalEach subject will receive treatment on Day 1 with Restylane Vital in one hand and the experimental device in the opposite hand, as randomly assigned

Timeline

Start date
2024-04-24
Primary completion
2024-06-28
Completion
2024-07-16
First posted
2024-04-18
Last updated
2025-10-10
Results posted
2025-10-10

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06372782. Inclusion in this directory is not an endorsement.