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

NCT02334358 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 503

Last updated 2019-03-13

Study results available
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Summary

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

Conditions

  • Correction of Nasolabial Folds

Interventions

DEVICE

YVOIRE Classic s

Sponsors & Collaborators

  • LG Life Sciences

    lead INDUSTRY

Principal Investigators

  • Q Li · Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2016-04-30
Completion
2016-08-31

Countries

  • China

Study Locations

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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 NCT02334358 on ClinicalTrials.gov