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Not Yet RecruitingNCT07412392

Study of DIOSHA S Lido Injection vs. YOUTHFILL Fine With Lidocaine in Treating Moderate to Severe Nasolabial Folds

A Multi Center, Randomized, Subject & Independent Evaluator-blinded, Matched Pairs, Active Controlled, Non-inferiority, Pivotal Study to Evaluate the Efficacy and Safety of Injection With DIOSHA S Lido as Compared to YOUTHFILL(YOUTHFILL Fine With Lidocaine) in Temporary Correction of Moderate to Severe Nasolabial Folds

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Hyundae Meditech · Industry
Sex
All
Age
19 Years – 75 Years
Healthy volunteers
Accepted

Summary

Study of DIOSHA S Lido Injection vs. YOUTHFILL Fine With Lidocaine in Treating Moderate to Severe Nasolabial Folds

Conditions

Interventions

TypeNameDescription
DEVICEDIOSHA S LidoInjection of a hyaluronic acid dermal filler containing lidocaine into the nasolabial folds for the temporary correction of moderate to severe nasolabial folds. Treatment is administered according to the study protocol, and participants are followed through Week 48 for efficacy and safety assessments.
DEVICEYOUTHFILL Fine with LidocaineInjection of a hyaluronic acid dermal filler containing lidocaine into the nasolabial folds for the temporary correction of moderate to severe nasolabial folds. Treatment is administered according to the study protocol, and participants are followed through Week 48 for efficacy and safety assessments.

Timeline

Start date
2026-02-27
Primary completion
2027-01-30
Completion
2027-07-30
First posted
2026-02-17
Last updated
2026-02-17

Source: ClinicalTrials.gov record NCT07412392. Inclusion in this directory is not an endorsement.