CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 148 enrolled
Drug / intervention
Restylane Defynedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03597256
NCT03597256N/ACompleted

A Randomized, Multi-center, Evaluator-blinded, No-treatment Controlled Study to Evaluate the Effectiveness and Safety of Restylane Defyne for Correction of Chin Retrusion

Galderma R&D·interventional·Posted Jul 24, 2018·Updated Jun 12, 2024

In Brief

A clinical study evaluating Restylane Defyne for Chin Retrusion. Completed, enrolled 148 participants across 1 site.

Detailed Summary

This is a randomized, evaluator-blinded, no-treatment controlled study in subjects with Chin Retrusion.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChin Retrusion
CountriesChina
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedJul 24, 2018
Enrollment StartOct 8, 2018
Primary CompletionSep 24, 2019
Study CompletionSep 9, 2020
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 7.9 years ago

Interventions

Restylane Defynedevice

Intradermal injection