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An Evaluation of the Clinical Utility and Safety of the Visant Medical Canalicular Plug

NCT04817085 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 156

Last updated 2022-06-06

No results posted yet for this study

Summary

This study is designed to evaluate the clinical utility and safety of the Visant Medical Canalicular Plug compared to a commercially available canalicular plug.

Conditions

  • Dry Eye

Interventions

DEVICE

Visant Medical Canalicular Plug

Plug is inserted into the inferior canaliculi and assessed for 6 months

DEVICE

Commercially available canalicular plug

Plug is inserted into the inferior canaliculi and assessed for 6 months

Sponsors & Collaborators

  • Visant Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Roger Albright · Ora Clinical Research Organization

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-06
Primary Completion
2022-02-09
Completion
2022-02-09
FDA Device
Yes

Countries

  • United States

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 NCT04817085 on ClinicalTrials.gov