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CompletedNCT05294562

China Post-Market Clinical Follow-up of FACILLE®

Status
Completed
Phase
Study type
Observational
Enrollment
1,552 (actual)
Sponsor
SciVision Biotech Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The results showed that subjects tolerated the Sodium Hyaluronate Gel for Injection (FACILLE®) well, with no systemic AEs, SAEs, and unanticipated AEs and associated with high satisfaction and self-evaluated effectiveness. Nearly half of the subjects maintained correction for 12 months and were satisfied with the product 3 years after the first injection.

Conditions

Timeline

Start date
2016-12-14
Primary completion
2017-05-07
Completion
2020-05-12
First posted
2022-03-24
Last updated
2022-03-24

Source: ClinicalTrials.gov record NCT05294562. Inclusion in this directory is not an endorsement.

China Post-Market Clinical Follow-up of FACILLE® (NCT05294562) · Clinical Trials Directory