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

This study has been withdrawn prior to enrollment.
(Lead researcher completed fellowship and never got study off ground)
Sponsor:
Information provided by:
University of California, San Diego
ClinicalTrials.gov Identifier:
NCT01059006
First received: January 28, 2010
Last updated: August 4, 2011
Last verified: August 2011
  Purpose

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.


Condition Intervention
Refractive Error
Presbyopia
Procedure: PresbyLASIK

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Peripheral PresbyLASIK Using the Allegretto Wavelight System For The Treatment of Presbyopia

Resource links provided by NLM:


Further study details as provided by University of California, San Diego:

Primary Outcome Measures:
  • Uncorrected near visual acuity [ Time Frame: 1 Day, 1 Week, 3 and 6 Months ] [ Designated as safety issue: No ]
  • Best corrected near visual acuity [ Time Frame: 1 Day, 1 Week, 3 and 6 Months ] [ Designated as safety issue: No ]
  • Intermediate visual acuity [ Time Frame: 1 Day, 1 Week, 3 and 6 Months ] [ Designated as safety issue: No ]
  • Stereoacuity test [ Time Frame: 1 Day, 1 Week, 3 and 6 Months ] [ Designated as safety issue: No ]
  • Psychometric questionnaire [ Time Frame: 1 Day, 1 Week, 3 and 6 Months ] [ Designated as safety issue: No ]

Enrollment: 0
Study Start Date: January 2010
Study Completion Date: July 2010
Primary Completion Date: July 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: PresbyLASIK
Male or female patients with presbyopic symptoms who underwent PresbyLASIK.
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.
Other Names:
  • Presbyopia
  • Presbyopic Symptoms

Detailed Description:

Presbyopia is a physiologic change related to age in which there is reduction in the eye's ability to focus in order to obtain clear vision for near distance. At approximately age 40 the range of accommodation begins to decrease and there is a diminishing capacity of the eye to focus on the nearest point it can focus on. This makes the need for corrective lenses a necessity in order to read at near as well as focus at an intermediate distance.

Presbyopia correction is one of the most frequently discussed topics in refractive surgery today. The idea of a creating a multifocal cornea using refractive surgery has sparked tremendous interest in finding a solution for this growing population throughout the world, especially amongst surgeons and the ophthalmic industry

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. PresbyLASIK is currently being offered routinely to patients in the San Diego area, across the country as well as in numerous centers around the world.

Conclusions from this study would serve as a guide for keratorefractive surgeons, who are pursuing peripheral PresbyLASIK, in determining the preoperative patient features in order to achieve the best outcome using the Wavelight-Allegretto System.

  Eligibility

Ages Eligible for Study:   35 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Male or female, of any race, and at least 35 to 80 years old with significant presbyopic symptoms at the time of the preoperative examination, and have signed an informed consent. The lower age limit of 35 is the earliest age in which reduction in accommodation occurs.
  • Refractive error between +3.00 to -5.00 diopters (D) sphere at the spectacle plane with no more than 3.00D of refractive astigmatism (negative cylinder format)
  • Best spectacle corrected visual acuity of at least 20/20 and J3 in both eyes.
  • Residual corneal bed thickness of ≥ to 330 microns
  • Demonstrated refractive stability, confirmed by clinical records. Neither the spherical nor the cylindrical portion of the refraction may have changed more than 0.50D during the 12-month period immediately preceding the baseline examination.
  • Soft contact lens users must have removed their lenses at least one week before baseline measurements. Hard contact lens users (PMMA or rigid gas permeable lenses) must have removed their lenses at least 4 weeks prior to baseline measurements and have two central keratometry readings and two manifest refractions taken at least one week apart that do not differ by more than 0.50 diopter in either meridian; mires should be regular.
  • Located in the greater San Diego area for a 6-month period.
  • Exhibit strong motivation for attending the follow-up visits.
  • Access to transportation to meet follow-up requirements.

Exclusion Criteria:

  • Patients that have previously been treated for refractive surgery (LASIK and/or PRK)
  • Patients with known history or have concurrent dry eye disease (e.g. keratoconjunctivitis sicca)
  • Patients who have less than 5 mm pupil size in dimlight
  • Female subjects who are pregnant, breast-feeding or intend to become pregnant during the first six months of the study.
  • Concurrent topical or systemic medications that may impair healing, including corticosteroids, antimetabolites, isotretinoin (Accutane), amiodarone hydrochloride (Cordarone) and/or sumatriptan (Imitrex) or any other triptan.
  • Medical condition(s), which, in the judgment of the investigator, may impair healing, including but not limited to: collagen vascular disease, autoimmune disease, immunodeficiency diseases, and ocular herpes zoster or simplex.
  • Active ophthalmic disease, neovascularization of the cornea within 1mm of the intended ablation zone, or lens opacity.
  • Evidence of glaucoma or an intraocular pressure greater than 22 mm Hg at baseline.
  • Evidence of keratoconus, corneal irregularity, or abnormal videokeratography in either eye.
  • Corneal thickness insufficient to allow the residual remaining stromal bed to be at least 300 microns in each eye. The residual stromal bed thickness will be determined by subtracting both the LASIK flap thickness and depth of the ablation from the total central corneal thickness measured by pachymetry
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01059006

Sponsors and Collaborators
University of California, San Diego
Investigators
Principal Investigator: David J Schanzlin, MD UCSD Shiley Eye Center
  More Information

Publications:
Responsible Party: David Schanzlin, MD, UCSD Shiley Eye Center
ClinicalTrials.gov Identifier: NCT01059006     History of Changes
Other Study ID Numbers: 091460
Study First Received: January 28, 2010
Last Updated: August 4, 2011
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, San Diego:
Reflective Surgery
Presbyopia
PresbyLASIK

Additional relevant MeSH terms:
Presbyopia
Refractive Errors
Eye Diseases

ClinicalTrials.gov processed this record on April 22, 2014