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LSH Silicone Hydrogel Soft Hydrophilic Contact Lens for Daily Wear

NCT01735045 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2012-11-28

No results posted yet for this study

Summary

This study is to evaluate the performance of the LSH (mangofilcon A) silicone hydrogel soft contact lenses when used as a daily wear contact lens for the correction of myopia.

Conditions

  • Myopia

Interventions

DEVICE

Lagado LSH (mangofilcon A) Soft (hydrophilic) Contact Lens

Daily Wear

DEVICE

Benz 3GX (hioxifilcon B) Soft (hydrophilic) Contact Lens

Sponsors & Collaborators

  • Szabocsik and Associates, Inc.

    lead INDUSTRY

Principal Investigators

  • John M Szabocsik, PhD

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2011-12-31
Completion
2012-01-31

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 NCT01735045 on ClinicalTrials.gov