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Trial registered on ANZCTR
Registration number
ACTRN12616001593426
Ethics application status
Approved
Date submitted
2/11/2016
Date registered
18/11/2016
Date last updated
6/04/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
The determinants of corneal curvature in healthy participants and in cataract surgery patients
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Scientific title
Analysis of corneal refractive power changes associated with accommodation, corneal biomechanics and cataract surgery
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Secondary ID [1]
290447
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cornea after Cataract surgery
300814
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Condition category
Condition code
Eye
300636
300636
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0
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Diseases / disorders of the eye
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
All the investigations involved in this study are non-invasive and non-contact procedures that are routinely used in clinical ophthalmology.
The first part of the study comparative diagnostic trial to compare clinical aberrometers. Participants will be examined on 4 different types of aberrometers (as described below) at a single half an hour long visit This part will commence in the first instance, approximately a month before the first cataract patient is assessed.
The second is non randomized observational trial to examine changes in corneal curvature associated with ocular accommodation assessed with corneal tomography and aberrometry and the relative influence of corneal biomechanics. Healthy participants will undergo corneal tomography and aberrometry, (Galilei 2 and Orbscan) and corneal biomehanics (Corvis-ST), as described below. The assessments will only take up to half an hour at a single visit. The second part will run concurrently with the third part of the study.
The final and arguably the most important part, is observational cohort study to characterise the relationship between corneal incision architecture and corneal biomechanics on two different incision sizes of surgically induced astigmatism following cataract surgery, using clinical aberrometry, corneal accommodation using tomography and corneal biomechanics. In this part, all the patients will be assessed at least a few hours once before the surgery, and 3 times after the surgery, which is standard of care for patients after cataract surgery. Assessments only take about 30 additional minutes more than their regular follow-up visit.
Visual acuity: Vision will be assessed using a letter chart. This is done as a standard of care for all the patients undergoing cataract surgery.
Slit-lamp biomicroscopy: Standard eye examination will be performed using a special microscope called a slit-lamp, which is used in every eye clinic room.
Aberrometry and tomography: The curvature of the front part of eye will be measured using special instruments known as the Orbscan II, Zywave, OPDIII, iDesign and Galilei 2 (only Galilei 2 for the third part). The instruments are used to assess the shape, refractive properties and thickness of cornea.
Biomechanical properties of cornea: The biomechanics (rigidity and flexibility) of the front part of your eye will be measured with a special instrument called Corvis-ST. This instrument also uses a gentle air puff for measurement. It does not cause any discomfort or pain to the eyes.
Optical Coherence Tomography: The instrument produces high resolution images the front of the eye with a special laser camera called anterior segment - Optical Coherence Tomographer (AS-OCT).
Specular microscopy: This technique is used to evaluate the health of corneal endothelium. The endothelial cell density will be quantified after obtaining clinical images.
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Intervention code [1]
296301
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Relationship between biomechanics of the cornea, using Corvis-ST, and surgically induced astigmatism, using tomographer (Galilei 2), following cataract surgery.
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Assessment method [1]
300047
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Timepoint [1]
300047
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Patients will be assessed at least a few hours before surgery, and, one day, one month and three months after the surgery.
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Primary outcome [2]
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Relationship between biomechanics of the cornea and wound architecture following cataract surgery. Biomechanics of the cornea will be measured by Corvis-ST and wound architecture by anterior segment optical coherence tomographer (AS-OCT) and Specular microscopy.
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Assessment method [2]
300076
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Timepoint [2]
300076
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Patients will be assessed at least a few hours before surgery, and, one day, one month and three months after surgery.
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Secondary outcome [1]
328919
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Topographical maps and corneal higher order aberrations obtained by 4 different aberrometers (Zywave, OPDIII, iTrace and Galilei 2) will be compared. This is a composite secondary outcome.
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Assessment method [1]
328919
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Timepoint [1]
328919
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This is the first part of the study. Three months from the commencement of the project.
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Eligibility
Key inclusion criteria
Part 1 and 2: Ametropia <1D (defocus or astigmatism). Participants can be healthy volunteers.
Part 3: Patients scheduled for routine cataract surgery.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Part 1: Ametropia >1D (defocus or astigmatism)
Part 1, 2 and 3: Pre-existing ocular pathology or previous ocular surgery, Contact lens use,
Strabismus, Previous ocular trauma
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Study design
Purpose
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Duration
Longitudinal
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Selection
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Timing
Prospective
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Statistical methods / analysis
All statistical analysis will be completed using the R statistical software package and Microsoft Excel.
Part 1: The difference in total and individual HOA will be investigated using basic plots to visualise the raw data, investigate outliers and the spread of the data. Analysis of variance (ANOVA) and multivariate analysis of variance (MANOVA) and canonical discriminat analysis will be used to compare HOA with post hoc tests where required. Non-normal data will be analysed using non-parametric tests.
Part 2: Statistical analysis will include analysis as described for Part 1 in addition to correlation and regression analysis to investigate the relationship between Corvis-ST data and accommodation induced corneal tomographic changes.
Part 3: Surgically induced astigmatism (SAI) will be calculated for all patients based on pre and post-operative tomography data using vector analysis. The relationship between SIA magnitude, corneal biomechanics, and corneal wound architecture will be modelled using regression analysis.
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
21/11/2016
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Actual
28/11/2016
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Date of last participant enrolment
Anticipated
1/11/2017
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Actual
1/12/2017
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Date of last data collection
Anticipated
28/09/2018
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Actual
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Sample size
Target
180
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Accrual to date
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Final
140
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Recruitment outside Australia
Country [1]
8366
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New Zealand
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State/province [1]
8366
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Auckland
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Funding & Sponsors
Funding source category [1]
294862
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University
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Name [1]
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The University of Auckland
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Address [1]
294862
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Department of Ophthalmology
New Zealand National Eye Centre
Faculty of Medical and Health Sciences
The University of Auckland,
Private Bag 92019
Auckland 1142
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Country [1]
294862
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New Zealand
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Primary sponsor type
University
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Name
The University of Auckland
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Address
Department of Ophthalmology
New Zealand National Eye Centre
Faculty of Medical and Health Sciences
The University of Auckland,
Private Bag 92019
Auckland 1142
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Country
New Zealand
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Secondary sponsor category [1]
293702
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None
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Name [1]
293702
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None
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Address [1]
293702
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None
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Country [1]
293702
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
296246
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Health and Disability Ethics Committee
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Ethics committee address [1]
296246
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Health and Disability Ethics Committees Ministry of Health Freyberg Building 20 Aitken Street PO Box 5013 Wellington 6011
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Ethics committee country [1]
296246
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New Zealand
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Date submitted for ethics approval [1]
296246
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02/09/2016
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Approval date [1]
296246
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22/09/2016
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Ethics approval number [1]
296246
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HDEC 16/CEN/132
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Summary
Brief summary
Following removal of a cataract, an intraocular lens (IOL) is implanted during surgery to enable refractive correction of the eye to maximise vision following surgery. Selecting the correct model and refractive power of the IOL is critical to achieve the appropriate refractive target. A sub-optimally selected IOL will typically result in post-operative residual refractive error, and decreased unaided vision that may be associated with falls and decreased quality of life in many cases. Refractive error is caused by the combined effect of the cornea and the lens and can be divided into lower order aberrations (LOA) and higher order aberrations (HOA). To select an appropriate model IOL to minimise total spherical aberration and accurate assessment of corneal aberration is required prior to surgery. The first part of this study will compare four clinical aberrometers that use different optical principals to assess HOA in the eye. Ocular accommodation is the process by which the crystalline lens adjusts the focus of the eye through conformational changes. A new strategy to accurately assess corneal curvature changes will be developed using 3D printed modifications to existing clinical tomographers and aberromters to allow corneal curvature assessment at near and distance fixation. Using this strategy even small changes in the corneal periphery should be quantifiable to definitively establish of the role of the cornea in accommodation. This is the second part of the project. Cataract surgery typically involves small incisions placed in the peripheral cornea to extract the cataract using phacoemulsification, and to enable implantation of an intraocular lens following cataract removal. The size of the corneal incisions depends on the IOL that is selected and the lens cartridge that is required for insertion. The final part of this study will aim to characterise the relative contribution of wound architecture and corneal biomechanics on surgically induced astigmatism.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr James McKelvie
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Address
69358
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Department of Ophthalmology
New Zealand National Eye Centre
Faculty of Medical and Health Sciences
The University of Auckland,
Private Bag 92019
Auckland 1142
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Country
69358
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New Zealand
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Phone
69358
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+64 9 923 6712
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Fax
69358
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Email
69358
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[email protected]
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Contact person for public queries
Name
69359
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James McKelvie
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Address
69359
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Department of Ophthalmology
New Zealand National Eye Centre
Faculty of Medical and Health Sciences
The University of Auckland,
Private Bag 92019
Auckland 1142
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Country
69359
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New Zealand
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Phone
69359
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+64 9 923 6712
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Fax
69359
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Email
69359
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[email protected]
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Contact person for scientific queries
Name
69360
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James McKelvie
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Address
69360
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Department of Ophthalmology
New Zealand National Eye Centre
Faculty of Medical and Health Sciences
The University of Auckland,
Private Bag 92019
Auckland 1142
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Country
69360
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New Zealand
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Phone
69360
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+64 9 923 6712
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Fax
69360
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Email
69360
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Current supporting documents:
Updated to:
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
23458
Other
Wallace, H. B., Misra, S. L., Li, S. S., & McKelvie, J. (2019). Biomechanical changes in the cornea following cataract surgery: A prospective assessment with the Corneal Visualisation Scheimpflug Technology. Clinical & experimental ophthalmology, 47(4), 461-468.
https://onlinelibrary.wiley.com/doi/full/10.1111/ceo.13451
23459
Other
Wallace, H. B., Misra, S. L., Li, S. S., & McKelvie, J. (2018). Predicting pseudophakic refractive error: Interplay of biometry prediction error, anterior chamber depth, and changes in corneal curvature. Journal of Cataract & Refractive Surgery, 44(9), 1123-1129.
https://www.sciencedirect.com/science/article/pii/S0886335018304905
23460
Other
Li, S. S., Misra, S. L., Wallace, H. B., & McKelvie, J. (2018). Effect of phacoemulsification incision size on incision repair and remodeling: Optical coherence tomography assessment. Journal of Cataract & Refractive Surgery, 44(11), 1336-1343.
https://www.sciencedirect.com/science/article/pii/S0886335018306321
23806
Other
The details of published peer-reviewed scientific ...
[
More Details
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Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Effect of phacoemulsification incision size on incision repair and remodeling: Optical coherence tomography assessment.
2018
https://dx.doi.org/10.1016/j.jcrs.2018.07.025
N.B. These documents automatically identified may not have been verified by the study sponsor.
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