Comparison of Femtosecond Laser Assisted Cataract Surgery to Conventional Phacoemulsification Cataract Surgery

Sponsor
Johns Hopkins University (Other)
Overall Status
Completed
CT.gov ID
NCT02096627
Collaborator
(none)
154
1
54
2.8

Study Details

Study Description

Brief Summary

In this project, the investigators aim to compare the safety, efficacy, and predictability outcomes of conventional CEIOL surgery to Femtosecond-laser-assisted CEIOL (FLACS) in an effort to improve cataract surgery outcomes. The investigators hypothesis is that FLACS may lead to preservation of endothelial cells compared to conventional CE IOL.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will only include patients who are eligible to undergo cataract surgery. All patients will receive treatment that is FDA approved for cataract surgery. Because all study participants will have been scheduled for elective cataract extraction regardless of their participation in this study, there will be little or no additional surgical risk associated with participation. A total of 720 patients are expected to be enrolled in the study during a period of 2 years. The investigators will recruit patients with bilateral operable cataracts. One eye will undergo cataract surgery using conventional cataract extraction technique including phacoemulsification whereas the second eye will undergo FLACS. No significant increased risk to the patient is expected in either arm of the study compared to routine cataract surgery. The patients will be examined as per previous post-operative cataract surgery guidelines on POD1, POW1, POM1, POM3, POM6, POY1 and POY2. The only treatment difference will take place at the time of the cataract surgery. Post-operatively, endothelial cell count will be obtained by the no-touch technology of specular microscopy at baseline as well as three months after surgery. If the study ends prematurely, the investigators do not anticipate any significant change in the care of the patient.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    154 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Comparison of Femtosecond Laser Assisted Cataract Surgery to Conventional Phacoemulsification Cataract Surgery on Corneal Endothelial Cell Loss
    Study Start Date :
    May 1, 2014
    Actual Primary Completion Date :
    Nov 1, 2018
    Actual Study Completion Date :
    Nov 1, 2018

    Arms and Interventions

    Arm Intervention/Treatment
    conventional

    Patients who undergo routine cataract surgery using conventional phacoemulsification technique

    FLACS

    Patients who undergo femtosecond laser assisted cataract surgery

    Outcome Measures

    Primary Outcome Measures

    1. endothelial cell density three months after conventional CEIOL or FLACS compared to baseline [up to 2 years]

      endothelial cell density will be compared at baseline and three months after a patient undergoes FLACS or Conventional CE IOL to see which technique causes less endothelial cell loss.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients older than 18 years of age

    2. Ability to understand and sign an informed consent

    3. Visually significant cataract eligible to undergo cataract extraction by phacoemulsification with primary intraocular lens implantation in at least 1 eye

    4. Ability and commitment to follow up for 18 months after surgery

    5. No other ocular pathology and no previous/concurrent surgery

    Exclusion Criteria:
    1. Any other ocular pathology that may affect best-corrected visual acuity

    2. Previous or concurrent ocular surgery

    3. Subjects who are pregnant, lactating, or planning to be pregnant during the course of the study.

    4. Patients with keratoconus or keratectasia

    5. Patients who are blind on one eye

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Johns Hopkins University Baltimore Maryland United States 21044

    Sponsors and Collaborators

    • Johns Hopkins University

    Investigators

    • Principal Investigator: yassine daoud, md, Johns Hopkins University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Johns Hopkins University
    ClinicalTrials.gov Identifier:
    NCT02096627
    Other Study ID Numbers:
    • NA_00089916
    First Posted:
    Mar 26, 2014
    Last Update Posted:
    Nov 16, 2018
    Last Verified:
    Nov 1, 2018
    Keywords provided by Johns Hopkins University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 16, 2018