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Performance of Toric Silicone Hydrogel Contact Lenses Following One Month of Daily Wear

NCT03418064 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2019-11-13

Study results available
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Summary

The aim of this prospective study is to evaluate the clinical performance of fanfilcon A toric and lotrafilcon B toric contact lenses after 1 month of wear in each pair.

Conditions

  • Astigmatism

Interventions

DEVICE

Fanfilcon A toric lens

Contact lens

DEVICE

Lotrafilcon B toric lens

Contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-10
Primary Completion
2018-05-16
Completion
2018-05-16
FDA Device
Yes

Countries

  • Mexico

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 NCT03418064 on ClinicalTrials.gov