MedTrace Logo

Peripheral PresbyLASIK Using the Allegretto Wavelight System For The Treatment of Presbyopia

NCT01059006 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2011-08-05

No results posted yet for this study

Summary

The aim of this study is to analyze the results of PresbyLASIK performed using the wavefront-optimized LASIK for the treatment of presbyopia on low hyperopic and low myopic patients with astigmatism. Visual performance will be assessed using clinical outcome measures of the following: refraction, near, intermediate and distance visual acuity, stereoacuity and contrast sensitivity. Questionnaires will also be used to evaluate how the patient's vision is before and after surgery.

Conditions

Interventions

PROCEDURE

PresbyLASIK

PresbyLASIK essentially involves the creation of a multifocal surface able to correct any visual defect for distance while simultaneously allowing freedom from near spectacle dependency in presbyopic patients.

Sponsors & Collaborators

Principal Investigators

  • David J Schanzlin, MD · UCSD Shiley Eye Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
35 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2010-07-31
Completion
2010-07-31

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01059006 on ClinicalTrials.gov