Evaluation of the Efficacy of Restylane Silk in the Correction of Tear Trough Deformity

NCT02689947 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-03-29

No results posted yet for this study

Summary

Prospective single center study to evaluate the safety and effectiveness of Restylane Silk for treatment of tear trough correction.

Conditions

  • Tear Trough Deformity

Interventions

DEVICE

Restylane Silk

Sponsors & Collaborators

  • Nashville Centre for Laser and Facial Surgery

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2017-03-31
Completion
2017-03-31

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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 NCT02689947 on ClinicalTrials.gov