At a glance
ClinicalIndex Comparison RecordN/ACompleted· 132 enrolled
Drug / intervention
Restylane Perlanedevice
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.
A Randomized, Open Label, No-treatment Controlled, Multi-center, Efficacy and Safety Study Using Restylane Perlane to Shape the Nasal Dorsum and/or Nasal Root
In Brief
A clinical study evaluating Restylane Perlane for Nasal Augmentation. Completed, enrolled 132 participants across 2 sites.
Detailed Summary
The purpose of this study is to determine the safety and efficacy of using Restylane Perlane to shape the nasal dorsum and/or nasal root in comparison with a no-treatment control group
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNasal Augmentation
CountriesChina
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedAug 2014
Enrollment StartSep 2014
Primary CompletionDec 2015
Study CompletionJun 2016
TodayJul 2026
First PostedAug 15, 2014
Enrollment StartSep 1, 2014
Primary CompletionDec 1, 2015
Study CompletionJun 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 11.9 years ago
Interventions
Restylane Perlanedevice
Intradermal injection