At a glance
ClinicalIndex Comparison RecordN/ACompleted· 48 enrolled
Drug / intervention
Princess® VOLUMEdevice
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.
Open-label Uncontrolled, Multicenter Study for the Evaluation of the Efficacy and Safety of the Dermal Filler Princess® VOLUME in Nasolabial Folds
In Brief
A clinical study evaluating Princess® VOLUME for Nasolabial Folds. Completed, enrolled 48 participants across 3 sites.
Detailed Summary
The aim of this clinical trial is to evaluate the efficacy and safety of Princess® VOLUME for the correction of nasolabial folds.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNasolabial Folds
CountriesAustria
CollaboratorsFGK Clinical Research GmbH
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedFeb 2013
Enrollment StartApr 2013
Primary CompletionApr 2014
Study CompletionJun 2014
TodayJul 2026
First PostedFeb 26, 2013
Enrollment StartApr 1, 2013
Primary CompletionApr 1, 2014
Study CompletionJun 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 13.3 years ago
Interventions
Princess® VOLUMEdevice