Skip to main content
OpenTrials
Completed

NCT Number: NCT02053688

Evaluation Study on Corneal Lens for Vision Correction

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cliff Leong, Fremont, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient with good corneal health
  • Age 18-65.
  • Patients able to understand the requirements of the study and willing to follow study instructions, to provide written informed consent to participate, and who agree to comply with all study requirements.
  • Best corrected visual acuity of 20/20 or better in the study eye/s

Exclusion criteria

  • Any other anterior segment abnormality.
  • No previous corneal procedures, including Laser Vision Correction.
  • Any abnormalities associated with the eye lids.
  • Clinically significant inflammation or infection within six (6) months prior to study.
  • Uncontrolled systemic disease (e.g., diabetes, hypertension, etc.) in the opinion of the Investigator.
  • Participation in any study involving an investigational drug or device within the past 30 calendar days, or ongoing participation in a study with an investigational material except studies using corneal lenses.
  • Intolerance or hypersensitivity to topical anesthetics, fluorescein, or components of the material.
  • Specifically known intolerance or hypersensitivity to contact lenses.
  • Any condition that, in the opinion of the investigator, would jeopardize the safety of the patient.

Treatment and study plan

Astigmatic Correction Lens (Nexis ACCL lenses)

Device

Astigmatic refractive error correction

Toric Soft Contact Lenses

Device

astigmatism correction using toric optics

Primary outcomes

  1. Visual Acuity

    Time frame: 30 mins

Sponsors and collaborators

Lead sponsor

FORSIGHT Vision3

Industry

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Feb 4, 2014
Registry last updated
Feb 4, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.