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Corneal Biomechanics, Optical Properties and Anterior Segment Structural Features in Patients With Pseudoexfoliation

NCT06731530 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 86

Last updated 2024-12-27

No results posted yet for this study

Summary

The purpose of this study is to assess the effect of pseudoexfoliation syndrome on corneal biomechanics, optical clarity of the cornea, and anterior segment structural features.

Conditions

  • Pseudoexfoliation Syndrome
  • Biomechanical Parameters
  • Corneal Densitometry

Interventions

DEVICE

Pentacam-AXL

Pentacam-AXL (Oculus, Wetzlar, Germany)

DEVICE

HD Analyzer

HD Analyzer (Visiometrics, Terassa, Spain, Keeler)

DEVICE

Corvis ST

Corvis ST (Oculus, Germany)

DEVICE

OCT-A Angiovue

OCT-A Angiovue (Optovue, Inc., Fremont, California, USA)

DEVICE

IOLMaster V.5.4

IOLMaster V.5.4 (Carl Zeiss., Meditec)

DEVICE

Topcon SP-1P

Topcon SP-1P (Topcon Medical Inc., Tokyo, Japan)

OTHER

BCVA (ETDRS), Slit lamp examination, Goldmann Applanation Tonometry, Fundus examination

BCVA (ETDRS), Slit lamp examination, Goldmann Applanation Tonometry, Fundus Examination

Sponsors & Collaborators

  • Papageorgiou General Hospital

    collaborator OTHER

  • Aristotle University Of Thessaloniki

    lead OTHER

Principal Investigators

  • Nikolaos Ziakas, Professor · Aristotle University Of Thessaloniki

Eligibility

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

Timeline & Regulatory

Start
2024-12-13
Primary Completion
2025-05-31
Completion
2025-05-31

Countries

  • Greece

Study Locations

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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 NCT06731530 on ClinicalTrials.gov