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Clinical Trials/NCT01884805
NCT01884805
Terminated
Not Applicable

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

University Hospital, Toulouse1 site in 1 country9 target enrollmentMarch 2013
ConditionsHyperopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hyperopia
Sponsor
University Hospital, Toulouse
Enrollment
9
Locations
1
Primary Endpoint
Measurement of optical aberrations
Status
Terminated
Last Updated
6 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
September 2013
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • hyperopic patients
  • to be able to understand an information and give a consent
  • affiliated to medical insurance

Exclusion Criteria

  • pregnant women or nursing mothers
  • ocular infection
  • keratitis
  • restless patients
  • ocular surgery 90 days before inclusion

Outcomes

Primary Outcomes

Measurement of optical aberrations

Time Frame: 1 day (Participants will be followed for the duration of ophtalmology consultation)

Feasibility of Measurement of optical aberrations in hyperopia by using an Adaptive Optics Visual Simulator AOVIS-I. Outcome measure is assessed during a consultation

Secondary Outcomes

  • Reproductibility of the measures(1 day (Participants will be followed for the duration of ophtalmology consultation))
  • Quantitative measurement of optical aberrations(1 day (Participants will be followed for the duration of ophtalmology consultation))

Study Sites (1)

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