Efficacy and Safety Study of SkinPlus-Hyal® to Nasolabial Fold

NACompletedINTERVENTIONAL
Enrollment

123

Participants

Timeline

Start Date

July 31, 2013

Primary Completion Date

January 31, 2014

Study Completion Date

March 31, 2014

Conditions
Wrinkle
Interventions
DEVICE

SkinPlus-Hyal®

The Injector will administer to the eligible subject the Study Device and Comparator Device (Comparator or Study Device) respectively to the left and right nasolabial fold in a randomized manner.

DEVICE

Restylane®

The Injector will administer to the eligible subject the Study Device and Comparator Device (Comparator or Study Device) respectively to the left and right nasolabial fold in a randomized manner.

Trial Locations (2)

463-707

Seoul national university Bundang Hospital, Seongnam-si

110-744

Seoul National University Hospital, Jongno-gu

All Listed Sponsors
collaborator

HumanTissueKorea Ltd.

UNKNOWN

lead

Seoul National University Hospital

OTHER

NCT01940575 - Efficacy and Safety Study of SkinPlus-Hyal® to Nasolabial Fold | Biotech Hunter | Biotech Hunter