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Completed Not applicable Interventional Results available

Restylane-L for Correction of Infraorbital Hollows

ClinicalTrials.gov ID: NCT04154930

Public ClinicalTrials.gov record NCT04154930. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 8:10 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Evaluator-blinded, Parallel Group, No-treatment Controlled, Multi-center Study to Evaluate the Safety and Effectiveness of Restylane-L® for Correction of Infraorbital Hollows

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective, randomized, evaluator-blinded, no-treatment controlled, parallel group, multi-center US study to evaluate the safety and effectiveness of Restylane-L® for correction of Infraorbital Hollows.

Study identification

NCT ID
NCT04154930
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Galderma R&D
Industry
Enrollment
333 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
22 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 10, 2019
Primary completion
Jan 30, 2021
Completion
Apr 5, 2022
Last update posted
Apr 24, 2023

2019 – 2022

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Galderma Research Site Encino California 91436
Galderma Research Site Los Angeles California 90069
Galderma Research Site Redondo Beach California 90277
Galderma Research Site Solana Beach California 92075
Galderma Research Site Westport Connecticut 06880
Galderma Research Site Boynton Beach Florida 33472
Galderma Research Site Coral Gables Florida 33146
Galderma Research Site West Palm Beach Florida 33401
Galderma Research Site Chicago Illinois 60654
Galderma Research Site Chestnut Hill Massachusetts 02467
Galderma Research Site New York New York 10003
Galderma Research Site New York New York 10021
Galderma Research Site Rochester New York 14564
Galderma Research Site Wilmington North Carolina 28405
Galderma Research Site Nashville Tennessee 37203
Galderma Research Site Spring Texas 77388

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04154930, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 24, 2023 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04154930 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →