Safety and Performance of DKL Crosslinked Sodium Hyaluronate 23 Dermal Filler for Improvement of NLF Appearance
NCT05021913 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48
Last updated 2023-07-05
Summary
This is a pivotal, prospective active-controlled, randomized, double blinded (blinded evaluator and subject), intra-individual split-face comparison, non-inferiority study of DKL crosslinked sodium hyaluronate 23 versus Juvederm Volift™ after injection into the mid to deep dermis for correction of moderate to deep nasolabial folds (NLFs).
Conditions
- Aging, Premature
Interventions
- DEVICE
-
DKL crosslinked sodium hyaluronate 23
is injected into the NLF on Day 1. The volume of injection will not exceed 2 mL per side. If applicable, a touch-up of DKL crosslinked sodium hyaluronate 23 will be injected on Day 30; the volume of injection will not exceed 1 mL per side.
- DEVICE
-
Juvéderm Volift™ with lidocaine (Allergan, Inc)
is injected into the NLF on Day 1. The volume of injection will not exceed 2 mL per side. If applicable, a touch-up of Juvéderm Volift™ will be injected on Day 30; the volume of injection will not exceed 1 mL per side.
Sponsors & Collaborators
-
CTC Clinical Trial Consultants AB
collaborator INDUSTRY -
Dr. Korman Laboratories Ltd.
lead INDUSTRY
Principal Investigators
-
Johan Nilsson, MD, PhD · CTC Clinical Trial Consultants AB
-
Mohammad Alimohammadi, MD, PhD · Almo Alo AB
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-08-20
- Primary Completion
- 2023-01-06
- Completion
- 2023-01-06
Countries
- Sweden
Study Locations
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