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NCT05342753 · ClinicalTrials.gov registry record · NA

Safety and Effectiveness of Restylane® Kysse for Lip Augmentation in Chinese Subjects

A NA study, sponsored by Galderma R&D.

Completed
Registry status
NA
Development phase
22
Enrollment target

NCT05342753: Completed NA study, sponsored by Galderma R&D.

NCT05342753 is a NA study that has completed, run by Galderma R&D. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05342753, a NA study, has completed, sponsored by Galderma R&D.

COMPLETED
Registry status
NA
Development phase
22 participants
Enrollment target

Study Summary

Open-label, phase IV, post-marketing study to evaluate aesthetic improvement in Chinese subjects after treatment with Restylane Kysse.

Primary Outcome

The MLFS is a validated photograph-based outcome instrument that is designed specifically for quantifying lip fullness. Scoring of lip fullness from Grade 1 to 5 (grade 1: "Very Thin", grade 2: "Thin", grade 3: "Medium", grade 4: "Full" and grade 5: "Very Full"; with a higher score reflecting greater lip fullness) was based on visual live assessment by the Investigator. Percentage of participants with at least 1-point improvement from baseline on MLFS are reported for this outcome measure.

Interventions

  • DEVICE Restylane Kysse

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2022-06-13
Est. Completion 2024-11-07
Phase NA
Galderma R&D

158 total trials

What the finished NCT05342753 record still lists

NCT05342753 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Restylane Kysse is the first listed.

NCT05342753 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05342753 about?

NCT05342753 is a clinical study titled "Safety and Effectiveness of Restylane® Kysse for Lip Augmentation in Chinese Subjects". Open-label, phase IV, post-marketing study to evaluate aesthetic improvement in Chinese subjects after treatment with Restylane Kysse.

What is the current status of trial NCT05342753?

This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2022-06-13. Estimated completion is 2024-11-07.

What interventions are being tested in trial NCT05342753?

The interventions under investigation include: Restylane Kysse (DEVICE).

Who is sponsoring clinical trial NCT05342753?

This trial is sponsored by Galderma R&D, which has 158 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05342753's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05342753, the US trial registry maintained by the National Library of Medicine. NCT05342753 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.