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Clinical Evaluation of a Silicone Hydrogel Lens

NCT01016132 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 152

Last updated 2012-06-29

Study results available
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Summary

The purpose of this study is to assess the performance of an investigational contact lens among contact lens wearers.

Conditions

  • Myopia

Interventions

DEVICE

lotrafilcon A contact lens

Investigational silicone hydrogel, single-vision, soft contact lens worn for four weeks at least as often as and on the same basis as participant's habitual lenses, as prescribed by participant's eye care practitioner -- ie., on a daily wear, flex wear, or extended wear basis.

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2009-12-31
Completion
2009-12-31

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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 NCT01016132 on ClinicalTrials.gov