Clinical Trials Directory

Trials / Completed

CompletedNCT05052242

Evaluation of Ocular Biometry in PACD With Two Swept Source Optical Coherence Tomography Devices

Evaluation of Ocular Biometry in Primary Angle-closure Disease With Two Swept Source Optical Coherence Tomography Devices

Status
Completed
Phase
Study type
Observational
Enrollment
45 (actual)
Sponsor
Department of Medical Services Ministry of Public Health of Thailand · Other Government
Sex
All
Age
40 Years – 77 Years
Healthy volunteers

Summary

Purpose: To investigate agreement between 2 swept source OCT biometers, IOL M.aster700 and Anterion, in various ocular biometry and intraocular lens (IOL) calculations of primary angle-closure disease (PACD). Methods: This was a prospective study conducted in a tertiary eye care centre involving biometric measurements obtained with 2 devices in phakic eye with diagnosis of PACD. Mean difference and intraclass correlation coefficient (ICC) with confidence limits were assessed, and calculations of estimated residual refraction of the IOL were analysed using Barrett's formula.

Detailed description

Primary angle-closure disease (PACD) is the leading cause of blindness worldwide. PACD is an anatomic disorder, typically of relatively small eye with shallow anterior chamber depth (ACD), thick lens, shorter axial length (AL), small corneal curvature, and relatively anterior lens position. Pupillary block, plateau iris and phacomorphic mechanisms play major roles in the pathophysiology of the disease, and pupillary block is thought to be the most common causal mechanism. For decades, phacoemulsification and intraocular lens implantation (PEI) has been proposed for initial management of PACD.4 PEI relieves pupillary block, deepening ACD and widening irido-corneal angle. Biometry is essential in evaluating ocular dimensions and calculating IOL power in PACD, and ocular biometers have been evolving in recent years. Optical coherence tomography (OCT) includes partial coherence interferometry (PCI), and swept source OCT (SS-OCT) is in general use in clinical practice. The agreement of the calculations of these devices has been studied by many investigators; however, research into their agreement in PACD patients has been sparse so far. A newer SS-OCT, Anterion, is now available and its performance needs to be evaluated.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTprimary angle closure disease2 swept source OCT biometers, IOL Master700 and Anterion

Timeline

Start date
2020-05-01
Primary completion
2021-08-31
Completion
2021-09-03
First posted
2021-09-22
Last updated
2021-09-22

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT05052242. Inclusion in this directory is not an endorsement.