CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 66 enrolled
Drug / intervention
Belotero Balance®device
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/NCT03777917
NCT03777917N/ACompleted

Pilot Study to Assess the Effectiveness and Safety of Belotero Balance® Injection for Volume Augmentation of the Infraorbital Hollow

Merz North America, Inc.·interventional·Posted Dec 17, 2018·Updated Nov 14, 2023

In Brief

A clinical study evaluating Belotero Balance® for Correction of Volume Loss in the Infraorbital Hollow Area. Completed, enrolled 66 participants across 3 sites.

Detailed Summary

The pilot study aims to define safety, effectiveness, and patient-reported outcomes for Belotero Balance® use in the infraorbital hollows.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedDec 17, 2018
Enrollment StartDec 27, 2018
Primary CompletionJun 18, 2019
Study CompletionMar 11, 2020
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 7.5 years ago

Interventions

Belotero Balance®device

Belotero® Balance for infraorbital hollows. Mode of application: subdermal injection.