Predicting the Lens Capsular Bag Size Using Pre-operative Biometry
Primary Purpose
Cataract Senile
Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Biometry
Sponsored by
About this trial
This is an interventional basic science trial for Cataract Senile focused on measuring capsular bag
Eligibility Criteria
Inclusion Criteria:
- Patient scheduled for cataract surgery
- Well dilated pupil at the pre-assessment visit (dilated pupil size at least 6.0mm)
- Age 21 and older
- Pre-operative visual acuity of at least 0.25 Snellen
Exclusion Criteria:
- Parameters that influence the capsular bag stability (pseudoexfoliation syndrome, St. p. severe eye trauma, Phakodonesis)
- In women of childbearing age, a pregnancy test will be performed before inclusion into the study.
Sites / Locations
- Hanusch Hospital, Department of Ophthalmology
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Capsular bag size
Arm Description
Lens thickness, lens shape, anterior chamber depth, axial eye length and angle-to-angle will be used as explanatory variables (independent variables) and the size of the capsular bag will be used as main outcome parameter (dependent variable). We will perform a multiple linear regression analysis (that allows determination of the overall fit (variance explained) of the model and the relative contribution of each of the predictors to the total variance explaine) between the independent and the dependent variable.
Outcomes
Primary Outcome Measures
Capsular bag size
• Prediction of the size of the post-operative capsular bag diameter using pre-operative optical biometry (lens thickness, lens shape, anterior chamber depth, axial eye length and angle-to-angle distance)
Secondary Outcome Measures
Full Information
NCT ID
NCT05578339
First Posted
January 30, 2022
Last Updated
October 12, 2022
Sponsor
Vienna Institute for Research in Ocular Surgery
1. Study Identification
Unique Protocol Identification Number
NCT05578339
Brief Title
Predicting the Lens Capsular Bag Size Using Pre-operative Biometry
Official Title
Predicting the Lens Capsular Bag Size Using Pre-operative Biometry
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
August 30, 2021 (Actual)
Study Completion Date
December 20, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vienna Institute for Research in Ocular Surgery
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aim of this study is to assess whether a high-resolution scan of the crystalline lens before surgery may be helpful in predicting post-operative capsule bag diameter.
Detailed Description
Most of the measurement procedures used in this study are non-invasive and all are used in standard routine clinical practice, the benefit/risk ratio appears acceptable.
However, a capsule tension ring will be used. A CTR is not used routinely, usually only in cataract operations in which the lens capsule is not stable enough - in other words, for stabilization. The insertion of the CTR is problem-free in most cases. In extremely rare cases, however, the lens capsule may be injured. And document complications will be collected, report them in a final paper. The CTR used in the study is a standard device and CE-marked device. Studies using CTR showed that it is beneficial in difficult cases.
Gonioscopy after cataract surgery will be performed after 1 week. At this time point the wound is already sealed and there appears to be no increased risk to the patient. In the first study performed in a similar fashion in 1999 gonioscopy was performed one day after surgery.
Aim of this study is to predict the diameter of the capsular bag using pre-operative optical biometry findings.
This is a prospective, observer-blind and monocentric study that includes patients scheduled for cataract surgery. Recruitment will take part on the day of pre-assessment. For each patient only one eye will be included.
In total 50 eyes of 50 patients will be included, of which at least 5 eyes with an axial eye length below 22.5mm and 5 eyes with an axial eye length above 25.0mm.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract Senile
Keywords
capsular bag
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Capsular bag size
Arm Type
Other
Arm Description
Lens thickness, lens shape, anterior chamber depth, axial eye length and angle-to-angle will be used as explanatory variables (independent variables) and the size of the capsular bag will be used as main outcome parameter (dependent variable).
We will perform a multiple linear regression analysis (that allows determination of the overall fit (variance explained) of the model and the relative contribution of each of the predictors to the total variance explaine) between the independent and the dependent variable.
Intervention Type
Device
Intervention Name(s)
Biometry
Intervention Description
Lens thickness, lens shape, anterior chamber depth, axial eye length and angle-to-angle will be used as explanatory variables (independent variables) and the size of the capsular bag will be used as main outcome parameter (dependent variable).
Primary Outcome Measure Information:
Title
Capsular bag size
Description
• Prediction of the size of the post-operative capsular bag diameter using pre-operative optical biometry (lens thickness, lens shape, anterior chamber depth, axial eye length and angle-to-angle distance)
Time Frame
2 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient scheduled for cataract surgery
Well dilated pupil at the pre-assessment visit (dilated pupil size at least 6.0mm)
Age 21 and older
Pre-operative visual acuity of at least 0.25 Snellen
Exclusion Criteria:
Parameters that influence the capsular bag stability (pseudoexfoliation syndrome, St. p. severe eye trauma, Phakodonesis)
In women of childbearing age, a pregnancy test will be performed before inclusion into the study.
Facility Information:
Facility Name
Hanusch Hospital, Department of Ophthalmology
City
Vienna
ZIP/Postal Code
1140
Country
Austria
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
all results will be published
Learn more about this trial
Predicting the Lens Capsular Bag Size Using Pre-operative Biometry
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