MedTrace Logo

Clinical Evaluation of Two Monthly Replacement Silicone Hydrogel Contact Lenses

NCT01629693 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 398

Last updated 2014-11-06

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate differences in the comfort at the end of the month between Air Optix® lenses versus Biofinity® lenses in habitual daily wear symptomatic soft contact lens wearers.

Conditions

  • Myopia
  • Astigmatism

Interventions

DEVICE

Lotrafilcon B contact lenses

Silicone hydrogel contact lenses (sphere or toric) per subject's habitual prescription

DEVICE

Comfilcon A contact lenses

Silicone hydrogel contact lenses (sphere or toric) per subject's habitual prescription

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Jami Kern, Ph.D. · Alcon Research

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2013-11-30
Completion
2013-11-30

More Related Trials

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 NCT01629693 on ClinicalTrials.gov