RecruitingNot ApplicableNCT07204691

A Study to Evaluate the Safety and Performance of Dr Korman Laboratories' Hyaluronic Acid Filler 20 mg/mL With Lidocaine for Lip Augmentation

A Single-arm, Open-label Clinical Investigation to Evaluate the Safety and Performance of DKL Crosslinked Sodium Hyaluronate 20 mg/mL + Lidocaine 0.3% Dermal Filler for Lip Augmentation


Sponsor

Dr. Korman Laboratories Ltd.

Enrollment

75 participants

Start Date

Sep 24, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study will assess the safety and effectiveness of a dermal filler called DKL crosslinked hyaluronic acid 20 mg/mL with lidocaine 0.3% when injected into the lips of healthy men and women who want to have fuller lips. The change in the appearance of the lips will be checked.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called DKL crosslinked sodium hyaluronate 20 mg/mL + Lidocaine 0.3% dermal filler for people with lip augmentation. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEDKL crosslinked sodium hyaluronate 20 mg/mL + Lidocaine 0.3% dermal filler

DKL crosslinked sodium hyaluronate 20 mg/mL + lidocaine 0.3% dermal filler is an injectable sterile, non-pyrogenic gel composed of crosslinked sodium hyaluronate of a non-animal origin and lidocaine in a phosphate-buffered saline solution.


Locations(2)

Clinical Trial Consultants AB (CTC) GoCo

Mölndal, Sweden

CTC Stockholm

Solna, Sweden

View Full Details on ClinicalTrials.gov

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NCT07204691