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A Study to Evaluate the Product Performance of a Low Add MultiFocal Soft Contact Lens

NCT01539694 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2020-09-30

Study results available
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Summary

The objective of this study is to evaluate the product performance of an investigational multifocal low add soft contact lens.

Conditions

Interventions

DEVICE

LD118033 contact lens

Multifocal contact lens worn on a daily wear basis for 1 week

DEVICE

PureVision multifocal contact lens

PureVision multifocal contact lens worn on a daily wear basis for 1 week.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Gerard Cairns, PhD, MCOptom · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2012-02-29
Completion
2012-03-31

Countries

  • United States

Study Locations

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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 NCT01539694 on ClinicalTrials.gov