Dispensing Study to Assess the Visual Performance of Optimised Prototype Contact Lenses

NCT02484586 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 161

Last updated 2017-09-11

No results posted yet for this study

Summary

The aim of this study is to assess the visual performance of multiple optimised prototype soft contact lens designs compared to commercially available contact lenses.

Conditions

Interventions

DEVICE

Etafilcon A

Prototype lens material

DEVICE

Etafilcon A

Control lens for presbyope group

DEVICE

Nelfilcon A

Control lens for presbyope group

DEVICE

Nesofilcon A

Control lens for presbyope group

DEVICE

Nelfilcon A

Control lens for non-presbyope group

DEVICE

Etafilcon A

Control lens for non-presbyope group

DEVICE

Somofilcon A

Control lens for presbyope group

DEVICE

58% Poly-HEMA

Control lens for presbyope group

DEVICE

Omafilcon A

Control lens for non-presbyope group

Sponsors & Collaborators

  • Brien Holden Vision

    lead INDUSTRY

Principal Investigators

  • Jennifer Sha, BOptom/BSc · Brien Holden Vision Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-10-31
Primary Completion
2017-02-07
Completion
2017-02-07

Countries

  • Australia

Study Locations

More Related Trials

Entities

Diseases

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 NCT02484586 on ClinicalTrials.gov