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Evaluation Study on Corneal Lens for Vision Correction

NCT02053688 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-02-04

No results posted yet for this study

Summary

The objective of this study is to evaluate the fitting and visual outcomes of Nexis Lens, made of silicone commonly used in the contact lens industry, on healthy eye with or without astigmatism.

Conditions

  • Astigmatism

Interventions

DEVICE

Astigmatic Correction Lens (Nexis ACCL lenses)

Astigmatic refractive error correction

DEVICE

Toric Soft Contact Lenses

astigmatism correction using toric optics

Sponsors & Collaborators

  • FORSIGHT Vision3

    lead INDUSTRY

Principal Investigators

  • Ashley Tuan, OD, PhD · Nexisvision

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2013-11-30
Completion
2013-12-31

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 NCT02053688 on ClinicalTrials.gov