Efficacy and Safety of Rejuviel V in the Correction of Midface Volume Deficit

NAActive, not recruitingINTERVENTIONAL
Enrollment

89

Participants

Timeline

Start Date

April 7, 2024

Primary Completion Date

March 8, 2026

Study Completion Date

March 30, 2026

Conditions
Mid-face Volume Deficit
Interventions
DEVICE

Rejuviel V® with lidocaine

Crosslinked hyaluronic acid (HA) 22 mg/mL + 0.3% lidocaine hydrochloride.

DEVICE

JUVEDERM® VOLUMA® with lidocaine

Crosslinked hyaluronic acid (HA) 20 mg/mL + 0.3% lidocaine hydrochloride.

Trial Locations (1)

Unknown

Chung-Ang University Hospital, Soeul

Sponsors
All Listed Sponsors
lead

PharmaResearch Co.,Ltd

INDUSTRY

NCT07162610 - Efficacy and Safety of Rejuviel V in the Correction of Midface Volume Deficit | Biotech Hunter | Biotech Hunter