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Evaluation of Safety and Tolerability of Ocular Lubricants

NCT05573360 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2023-07-06

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety profile of test formulations for an artificial tear product versus a comparator product.

Conditions

  • Dry Eye

Interventions

OTHER

NGF5-A test formulation

One drop of investigational product instilled on the eye

OTHER

NGF4-B test formulation

One drop of investigational product instilled on the eye

OTHER

NGF6-B test formulation

One drop of investigational product instilled on the eye

OTHER

NGF6-E test formulation

One drop of investigational product instilled on the eye

OTHER

Systane eye drop

One drop of commercial product instilled on the eye

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Lead, Dry Eye · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-16
Primary Completion
2023-05-31
Completion
2023-05-31

Countries

  • Australia

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 NCT05573360 on ClinicalTrials.gov