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Comparative Performance of PureVision Lens Designs

NCT00661687 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 206

Last updated 2011-12-12

Study results available
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Summary

The objective of this study is to evaluate the performance of the PureVision Lens designs when worn on a 30-day continuous wear basis

Conditions

  • Myopia

Interventions

DEVICE

Currently Marketed PureVision Contact Lens.

Contact lens for continuous wear

DEVICE

Alternate Design of the PureVision Contact Lens.

Contact lens for continuous wear

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

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

  • Benny Chian, MCOptom · Laser Focus Sdn Bhd, Vision Correction Centre

  • Harvey Siy Uy, MD · Asian Eye Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-02-29
Completion
2008-06-30

Countries

  • Malaysia
  • Philippines

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 NCT00661687 on ClinicalTrials.gov