Clinical Trials Directory

Trials / Terminated

TerminatedNCT01884805

Feasibility of Measurement of Optical Aberrations in Hyperopia by Using an Adaptive Optics Visual Simulator (AOVIS-I)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
9 (actual)
Sponsor
University Hospital, Toulouse · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of the protocol is to evaluate the adaptive optics visual simulator to measure optical aberrations in hyperopic eyes. The study hypotheses are the: * Ability to measure optical aberrations in hypermetropia. * Knowledge of optical aberrations of the eye hyperopic. * To adapt therapeutic management in optical aberrations measured.

Detailed description

The procedure is guided by the custom made software and its graphical user interface. The interface has been designed to be user-friendly, being very similar to the software usually managed by the clinicians in their daily professional practice. The complete procedure in one patient takes less than 5 minutes and is completely non-invasive. The optical measurements only involve the use of low power infrared laser and the visual testing is as simple for the patients as watching television and making responses.

Conditions

Interventions

TypeNameDescription
DEVICEMonocular Adaptive Optics Visual Simulator (AOVIS-I)The procedure is guided by the custom made software and its graphical user interface. The interface has been designed to be user-friendly, being very similar to the software usually managed by the clinicians in their daily professional practice. The complete procedure in one patient takes less than 5 minutes and is completely non-invasive. The optical measurements only involve the use of low power infrared laser and the visual testing is as simple for the patients as watching television and making responses.

Timeline

Start date
2013-03-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2013-06-24
Last updated
2019-07-16

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01884805. Inclusion in this directory is not an endorsement.