Status:
TERMINATED
Feasibility of Measurement of Optical Aberrations in Hyperopia by Using an Adaptive Optics Visual Simulator (AOVIS-I)
Lead Sponsor:
University Hospital, Toulouse
Collaborating Sponsors:
Centre de Référence National du Kératocône
Conditions:
Hyperopia
Eligibility:
All Genders
18+ years
Phase:
NA
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 a...
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 cli...
Eligibility Criteria
Inclusion
- hyperopic patients
- to be able to understand an information and give a consent
- affiliated to medical insurance
Exclusion
- pregnant women or nursing mothers
- ocular infection
- keratitis
- restless patients
- ocular surgery 90 days before inclusion
Key Trial Info
Start Date :
March 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2013
Estimated Enrollment :
9 Patients enrolled
Trial Details
Trial ID
NCT01884805
Start Date
March 1 2013
End Date
September 1 2013
Last Update
July 16 2019
Active Locations (1)
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1
University Hospital, Toulouse
Toulouse, Midi-Pyrenees, France, 31059