Evaluate the Effectiveness and Safety of Restylane Volyme in the Treatment of Temple Hollowing
NCT06665477 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 162
Last updated 2025-01-17
Summary
A randomized, no-treatment-controlled, evaluator-blinded, multi-center study to evaluate the effectiveness and safety of Restylane Volyme in the treatment of temple hollowing
Conditions
- Temple Hollowing
Interventions
- DEVICE
-
Restylane Volyme
Subjects in Restylane Volyme treatment group will receive treatment on Day 1 and optiponal treatment 1 month later.
Sponsors & Collaborators
-
Galderma R&D
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-11-18
- Primary Completion
- 2025-12-31
- Completion
- 2026-07-31
Countries
- China
Study Locations
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