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Clinical Evaluation of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract

Primary Purpose

Cataract Extraction

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Intraocular caliper-assisted capsulotomy
Verion navigation system-assisted capsulotomy
Sponsored by
Zhongshan Ophthalmic Center, Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Cataract Extraction

Eligibility Criteria

55 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults aged 55 to 80 years with age-related cataract;
  • Pupil diameter ≥ 6.5mm after pupil dilation;
  • Lens nuclear opacity grading score (LOCS III) lower than 4.0.

Exclusion Criteria:

  • Patients had previous intraocular surgery;
  • Patients with a diagnosed eye disease that may affect the functions of lens suspensory ligament such as previous ocular trauma, lens subluxation, pseudoexfoliation syndrome, retinal pigment degeneration;
  • Patients had other ocular diseases that impair visual function include optic neuropathy, uveitis, and tumor.
  • Refused to participate the study.

Sites / Locations

  • Zhongshan Ophthalmic Center,Sun Yat-Sen University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intraocular caliper-assisted capsulotomy group

Verion navigation system-assisted capsulotomy group

Arm Description

In intraocular caliper-assisted capsulotomy group, a modified intraocular caliper with standard calibration on the rinse needle was used to measure and locate the position of capsulorhexis with 5.3 mm diameter and the principle of pupillary margin in concentric circles. The surgeon could gently use the blunt needle in the front of the intraocular caliper to further make corresponding markers on the lens anterior capsule, and then carry out capsulotomy according to the marks.

In the Verion-assisted capsulotomy group, Verion navigation system was applied to project a 5.3 mm capsulorhexis centered on the corneal vertex. According to the projected capsulorhexis, capsulotomy was performed.

Outcomes

Primary Outcome Measures

Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm)
Images of the edges of IOL and capsulorhexis are taken at the end of the operation. Image J image analysis software is used to measure the horizontal diameter and vertical diameter of capsulorhexis with the diameter of IOL optical surface (6 mm) as the reference by two independently professional graders at the meantime, and further calculate the deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm) .

Secondary Outcome Measures

Uncorrected and corrected visual acuity
Visual acuity is evaluated with ETDRS visual acuity chart.
Ideal ratio of capsulorhexis
Ideal capsulorhexis is defined as a centered and round capsulorhexis, which can cover the edge of IOL optical surface continuously for 360 degrees with a diameter between 5.0 to 5.5 mm.
Grades of capsulorhexis-IOL overlap
The capsulorhexis-IOL overlap of each patient is graded as 360-degree continuous overlap, 270~360-degree overlap, 180~270-degree overlap, 90~180-degree overlap, and < 90-degree overlap.
Distance between pupil center and capsulorhexis center
Measured by Image J image analysis software.
Horizontal and vertical diameter of capsulorhexis
Measured by Image J image analysis software.
Intraocular lens tilt
Measured by anterior segment OCT (CASIA2).
Intraocular lens decentration
Measured by anterior segment OCT (CASIA2).
Intraocular aberrations
Measured by OPD-SCAN III.
Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm)

Full Information

First Posted
July 15, 2021
Last Updated
July 20, 2021
Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT04977115
Brief Title
Clinical Evaluation of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract
Official Title
Comparison of Intraocular Caliper-assisted and Verion Navigation System-assisted Capsulotomy in Phacoemulsification Surgery: A Randomized Non-inferiority Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 26, 2021 (Anticipated)
Primary Completion Date
February 28, 2022 (Anticipated)
Study Completion Date
April 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to compare the accuracy of capsulotomy assisted by intraocular caliper and Verion navigation system in phacoemulsification surgery and postoperative visual quality of patients.
Detailed Description
Continuous curvilinear capsulorhexis (CCC) is an important and technically challenging procedure in cataract surgery. However, most surgeons perform CCC by experience or referring to the pupil size, which is highly subjective and the accuracy of capsulorhexis is unsatisfactory. The investigators developed a new modified intraocular caliper with standard calibration on the rinse needle, which can measure and locate the position of capsulorhexis. The surgeon can gently use the blunt needle in the front of the intraocular caliper to further make corresponding markers on the lens anterior capsule, and then carry out capsulotomy according to the marks. We found intraocular caliper-assisted capsulotomy can obviously improve the accuracy of capsulorhexis. The purpose of this study is to compare the accuracy and postoperative visual quality of intraocular caliper-assisted capsulotomy with those of digital image projection device VERION navigation system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract Extraction

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
156 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intraocular caliper-assisted capsulotomy group
Arm Type
Experimental
Arm Description
In intraocular caliper-assisted capsulotomy group, a modified intraocular caliper with standard calibration on the rinse needle was used to measure and locate the position of capsulorhexis with 5.3 mm diameter and the principle of pupillary margin in concentric circles. The surgeon could gently use the blunt needle in the front of the intraocular caliper to further make corresponding markers on the lens anterior capsule, and then carry out capsulotomy according to the marks.
Arm Title
Verion navigation system-assisted capsulotomy group
Arm Type
Active Comparator
Arm Description
In the Verion-assisted capsulotomy group, Verion navigation system was applied to project a 5.3 mm capsulorhexis centered on the corneal vertex. According to the projected capsulorhexis, capsulotomy was performed.
Intervention Type
Procedure
Intervention Name(s)
Intraocular caliper-assisted capsulotomy
Intervention Description
Intraocular caliper is a modified intraocular caliper with standard calibration on the rinse needle.
Intervention Type
Procedure
Intervention Name(s)
Verion navigation system-assisted capsulotomy
Intervention Description
Verion Image Guided System (Alcon Laboratories, Inc.) is a digital image guidance system consisting of a diagnostic reference unit and a surgery pilot for intraoperative surgical assistance. The device can be used to align toric intraocular lens during surgery as well as support manual creation of a capsulorhexis with a predefined target diameter.
Primary Outcome Measure Information:
Title
Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm)
Description
Images of the edges of IOL and capsulorhexis are taken at the end of the operation. Image J image analysis software is used to measure the horizontal diameter and vertical diameter of capsulorhexis with the diameter of IOL optical surface (6 mm) as the reference by two independently professional graders at the meantime, and further calculate the deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm) .
Time Frame
During the surgery
Secondary Outcome Measure Information:
Title
Uncorrected and corrected visual acuity
Description
Visual acuity is evaluated with ETDRS visual acuity chart.
Time Frame
One month after surgery
Title
Ideal ratio of capsulorhexis
Description
Ideal capsulorhexis is defined as a centered and round capsulorhexis, which can cover the edge of IOL optical surface continuously for 360 degrees with a diameter between 5.0 to 5.5 mm.
Time Frame
During the surgery
Title
Grades of capsulorhexis-IOL overlap
Description
The capsulorhexis-IOL overlap of each patient is graded as 360-degree continuous overlap, 270~360-degree overlap, 180~270-degree overlap, 90~180-degree overlap, and < 90-degree overlap.
Time Frame
During the surgery
Title
Distance between pupil center and capsulorhexis center
Description
Measured by Image J image analysis software.
Time Frame
During the surgery
Title
Horizontal and vertical diameter of capsulorhexis
Description
Measured by Image J image analysis software.
Time Frame
During the surgery
Title
Intraocular lens tilt
Description
Measured by anterior segment OCT (CASIA2).
Time Frame
One month after surgery
Title
Intraocular lens decentration
Description
Measured by anterior segment OCT (CASIA2).
Time Frame
One month after surgery
Title
Intraocular aberrations
Description
Measured by OPD-SCAN III.
Time Frame
One month after surgery
Title
Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm)
Time Frame
One month after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults aged 55 to 80 years with age-related cataract; Pupil diameter ≥ 6.5mm after pupil dilation; Lens nuclear opacity grading score (LOCS III) lower than 4.0. Exclusion Criteria: Patients had previous intraocular surgery; Patients with a diagnosed eye disease that may affect the functions of lens suspensory ligament such as previous ocular trauma, lens subluxation, pseudoexfoliation syndrome, retinal pigment degeneration; Patients had other ocular diseases that impair visual function include optic neuropathy, uveitis, and tumor. Refused to participate the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaoyun Chen, PhD
Phone
+86 13632343642
Email
chenxiaoyun@gzzoc.com
Facility Information:
Facility Name
Zhongshan Ophthalmic Center,Sun Yat-Sen University
City
Guangzhou
ZIP/Postal Code
510060
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaoyun Chen, PhD
Phone
+86 13632343642
Email
chenxiaoyun@gzzoc.com

12. IPD Sharing Statement

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Clinical Evaluation of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract

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