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Ocular Comfort and OCT Observation of Post Lens Clearance and Ocular Tissue Compression

NCT01423773 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2013-06-28

Study results available
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Summary

The purpose of this study was to compare the fit and comfort of two types of contact lenses.

Conditions

  • Ocular Comfort

Interventions

DEVICE

Lotrafilcon A test contact lens

Silicone hydrogel single vision, soft contact lens with alternate parameters

DEVICE

Lotrafilcon A control contact lens

Silicone hydrogel single vision, soft contact lens

DEVICE

Ultra-High Resolution Optical Coherence Tomographer (OCT)

Investigational, nonsignificant risk device for measuring post lens clearance and ocular tissue compression during contact lens wear

Sponsors & Collaborators

  • Bascom Palmer Eye Institute

    collaborator OTHER

  • CIBA VISION

    lead INDUSTRY

Principal Investigators

  • Jianhua Wang, MD, PhD · Bascom Palmer Eye Institute

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2011-12-31
Completion
2011-12-31

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 NCT01423773 on ClinicalTrials.gov