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Pseudoexfoliation Syndrome in Myopes

Sponsor
General Hospital Sveti Duh (Other)
Overall Status
Completed
CT.gov ID
NCT01637740
Collaborator
(none)
5,753
Enrollment
29
Duration (Months)

Study Details

Study Description

Brief Summary

A retrospective study of 5753 eyes of cataract surgery patients was conducted at our Clinic. Ocular optical components measured by optical low coherence reflectometry biometer LENSTAR LS 900® of the cataract myopic eyes with pseudoexfoliation syndrome were put in comparison with those of cataract myopic eyes group without pseudoexfoliation syndrome.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    A retrospective study of 5753 eyes of cataract surgery patients was conducted at investigators Clinic in a period of 2.5 years. Pseudoexfoliation syndrome was found in 255 eyes. There were only 26 cataract myopic eyes with pseudoexfoliation syndrome. Refractive eye state was defined by preoperatively calculated emmetropization intraocular lens (IOL) value done by optical low coherence reflectometry biometer LENSTAR LS 900®. Ocular optical components of the cataract myopic eyes with pseudoexfoliation syndrome measured by this biometer were put in comparison with matched cataract myopic eyes group without pseudoexfoliation syndrome that have emmetropization IOL value within the same range as the cataract myopic eyes with pseudoexfoliation syndrome.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    5753 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Official Title:
    Pseudoexfoliation Syndrome in Myopes Defined With Optical Low Coherence Reflectometry
    Study Start Date :
    Aug 1, 2009
    Actual Primary Completion Date :
    Jan 1, 2012
    Actual Study Completion Date :
    Jan 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    eyes with pseudoexfoliation syndrome

    cataract myopic eyes with pseudoexfoliation syndrome
    eyes without pseudoexfoliation syndrome

    cataract myopic eyes without pseudoexfoliation syndrome

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      40 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • cataract surgery patients ≥ 40 years old
      Exclusion Criteria:
      • cataract surgery patients < 40 years old

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • General Hospital Sveti Duh

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Mladen Busic, M.D., PhD, General Hospital Sveti Duh
      ClinicalTrials.gov Identifier:
      NCT01637740
      Other Study ID Numbers:
      • 04072012MB
      • 04072012UECUHSD
      First Posted:
      Jul 11, 2012
      Last Update Posted:
      Jul 11, 2012
      Last Verified:
      Jul 1, 2012
      Keywords provided by Mladen Busic, M.D., PhD, General Hospital Sveti Duh
      myopia
      pseudoexfoliation syndrome
      optical low coherence reflectometry
      ocular optical components
      cataract
      Additional relevant MeSH terms:
      Cataract
      Exfoliation Syndrome
      Syndrome

      Study Results

      No Results Posted as of Jul 11, 2012