Clinical Trials Directory

Trials / Completed

CompletedNCT02055404

On-Eye Evaluation of Contact Lens Rotation Marks

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
3 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study was to select the size of the molded rotation mark for a new toric contact lens by comparing the visibility of various molded rotation marks.

Detailed description

Participants wore the test and control products contralaterally (in each eye separately) for 2 hours, during which the Investigator assessed the various molded rotation marks for visibility. Each participant was assessed by 10 investigators.

Conditions

Interventions

TypeNameDescription
DEVICEDelefilcon A spherical contact lens with molded marksSilicone hydrogel contact lens with 9 different molded marks of varying widths and depths indented into the front surface (S1, S2, S3, S4, S5, S6, S7, S8, and S9). Each lens contained all 9 marks.
DEVICEEtafilcon A toric contact lensHydrogel toric contact lens for daily wear, daily disposable use

Timeline

Start date
2013-02-01
Primary completion
2013-02-01
Completion
2013-02-01
First posted
2014-02-05
Last updated
2014-04-02
Results posted
2014-04-02

Source: ClinicalTrials.gov record NCT02055404. Inclusion in this directory is not an endorsement.

On-Eye Evaluation of Contact Lens Rotation Marks (NCT02055404) · Clinical Trials Directory