- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05915429
Predicting Lens Tilt Using Optical Coherence Tomography and Partial Least Squares Regression Modelling (Tilt)
Predicting Post-operative Intraocular Lens Tilt Using Optical Coherence Tomography Measurements and Partial Least Squares Regression Modelling
Misalignment of IOLs can cause severe loss of visual quality. Different types of misalignment are known. Tilt is one type of misalignment that is thought to play a negative role for the optical performance in eyes with IOL designs, especially, if they have aspheric, toric or multifocal optics.
Due to the fact that tilt has an influence on visual quality, the prediction of the post-operative tilt could improve IOL power calculaton significantly especially for toric IOLs. the Aim of this study is to measure tilt with two modern OCT based devices and one Scheimpflug camera and to predict the post-operative tilt using partial least squares regression.
Study Overview
Status
Conditions
Detailed Description
During cataract surgery an artificial intraocular lens (IOL) is implanted in the eye to replace the lens and to correct the refraction for distance vision. Misalignment of IOLs can cause severe loss of visual quality. Different types of misalignment are known. Tilt, one type of IOL misalignment is thought to play a negative role for the optical performance in eyes with IOL designs, especially, if they have aspheric, toric, or multifocal optics. For example, in the case of aspheric IOLs, it appears that even slight amount of tilt may result not only in the loss of the effect of reducing spherical aberrations but in more severe cases even a worsening of the optical quality compared to spherical IOLs. In the case of toric IOLs, tilt introduces higher order aberrations potentially mimicking astigmatism. In the case of multifocal IOLs, tilt increases higher order aberrations, which leads to decreased visual quality.
Various methods to measure IOL misalignments have been described. Studies assessing the IOL position have used subjective grading methods at the slit lamp examination or a Scheimpflug camera 2 to assess IOL decentration and tilt. The subjective grading at the slitlamp may display considerable variability between examiners. This method is more qualitative than quantitative and does not allow fine resolution when reporting IOL tilt. The fact that the patient has no standardized target to focus on makes the method even less reliable. Scanning methods such as Scheimpflug photos require a very well dilated pupil exceeding 6mm to assess the IOL position. Additionally, it can be difficult to identify the anatomical structures of the eye that need to be used as points of reference. 3 Scheimpflug camera images have been used for assessing IOL tilt previously, but erroneous results, often due to corneal magnification, have diminished their widespread use. Another possibility to assess tilt is the use of Purkinje reflexes. The light reflections of Purkinje images at ocular surfaces to evaluate ocular alignment have recently been utilized. Since light is reflected at all interfaces of media with a difference in refractive index, these reflections, called Purkinje images, can be used to assess tilt and decentration of IOLs. Two different clinically applicable Purkinjemeter system provide the measurement of IOL decentration and tilt. The main problem with Purkinje meters is accessibility, as there are only a few prototypes available worldwide.
The most recently developed method for tilt quantification is the use of optical coherence tomography. This method has several advantages compared to the previous methods: OCT based devices are available in most clinics, the resolution of modern OCT devices is high, and the measurements are reproducible.
Due to the fact that tilt has an influence on visual quality, the prediction of the post-operative tilt could improve IOL power calculation significantly, especially for toric IOLs. In the literature, the prediction of tilt was shown to be acceptable for the orientation of tilt, but not for the amount of tilt. Furthermore, there is disagreement concerning the fact, if the amount of tilt increases or decreases after cataract surgery. Aim of this study is to measure tilt with two modern OCT based devices and one Scheimpflug camera and to predict the post-operative tilt using partial least squares regression. This method was developed by Wold and introduced to ophthalmology previously.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Upper Austria
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Linz, Upper Austria, Austria, 4021
- Kepler University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- planned cataract surgery in one or both eyes
- above 21 years of age
Exclusion Criteria:
- Combined surgery (cataract plus glaucoma/vitreoretinal/corneal surgery)
- Best corrected distance visual acuity below 0.05 Snellen
- Pathologies that could have an influence on the post-operative tilt, such as pseudoexfoliation syndrome or previous ophthalmic trauma, or other reasons for phakodonesis.
- Previous ophthalmic surgery that could have an influence on post-operative tilt such as pars plana vitrectomy
- In case of pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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change of amount of tilt
Time Frame: preoperation visit and 8 weeks postoperation visit
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difference between preoperative amount of tilt in degrees and postoperative tilt in degrees
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preoperation visit and 8 weeks postoperation visit
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change of orientation of tilt in degrees
Time Frame: pre operation visit and 8 weeks post operation visit
|
differnece between preoperative orientation of tilt in degrees and postoperative orientation of tilt in degrees
|
pre operation visit and 8 weeks post operation visit
|
|
axial eye length
Time Frame: pre operation visit and 8 weeks post operation visit
|
axial eye length in mm
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pre operation visit and 8 weeks post operation visit
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anterior chamber depth
Time Frame: pre operation visit and 8 weeks post operation visit
|
anterior chamber depth in mm
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pre operation visit and 8 weeks post operation visit
|
|
anterior segment
Time Frame: pre operation visit and 8 weeks post operation visit
|
anterior segment (epithelium of the cornea to posterior lens capsule) in mm
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pre operation visit and 8 weeks post operation visit
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lens thickness
Time Frame: pre operation visit and 8 weeks post operation visit
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lens thickness in mm
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pre operation visit and 8 weeks post operation visit
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lens diameter
Time Frame: pre operation visit and 8 weeks post operation visit
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estimated lens diameter in mm
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pre operation visit and 8 weeks post operation visit
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|
shape factor
Time Frame: pre operation visit and 8 weeks post operation visit
|
shape of factor of the lens in mm
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pre operation visit and 8 weeks post operation visit
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|
corneal radii
Time Frame: pre operation visit and 8 weeks post operation visit
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corneal radii in mm
|
pre operation visit and 8 weeks post operation visit
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age
Time Frame: pre operation visit and 8 weeks post operation visit
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age in years
|
pre operation visit and 8 weeks post operation visit
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Collaborators and Investigators
Investigators
- Principal Investigator: Matthias Bolz, MD, JKU Linz
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KUK-Ophthalmology-004
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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