Observational Study to Evaluate Long-term Safety and Biodegradability of YVOIRE Volume s

NCT02661737 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 503

Last updated 2019-03-19

Study results available
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Summary

To evaluate long-term safety of YVOIRE volume s by incidence of adverse events including injection site local reactions and biodegradability.

Conditions

  • Correction of Nasolabial Folds

Interventions

DEVICE

YVOIRE volume s

Sponsors & Collaborators

  • LG Life Sciences

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2017-04-30
Completion
2017-09-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02661737 on ClinicalTrials.gov