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Performance of Toric Silicone Hydrogel Contact Lenses

NCT05097144 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-10-17

Study results available
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Summary

The purpose of this study was to evaluate the clinical performance and subjective lens handling (insertion and removal) of two toric silicone hydrogel contact lenses after one month of daily wear each.

Conditions

  • Astigmatism
  • Myopia

Interventions

DEVICE

Lens A (fanfilcon A)

Daily wear for one month

DEVICE

Lens B (asmofilcon A)

Daily wear for one month

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Rubén Velázquez Guerrero, MSc, FIACLE · National Autonomous University (UNAM)

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
2021-08-21
Primary Completion
2021-12-08
Completion
2021-12-08
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 NCT05097144 on ClinicalTrials.gov