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

Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04977115
Collaborator
(none)
156
1
2
9.1
17.1

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intraocular caliper-assisted capsulotomy
  • Procedure: Verion navigation system-assisted capsulotomy
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
156 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Comparison of Intraocular Caliper-assisted and Verion Navigation System-assisted Capsulotomy in Phacoemulsification Surgery: A Randomized Non-inferiority Trial
Anticipated Study Start Date :
Jul 26, 2021
Anticipated Primary Completion Date :
Feb 28, 2022
Anticipated Study Completion Date :
Apr 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intraocular caliper-assisted capsulotomy group

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.

Procedure: Intraocular caliper-assisted capsulotomy
Intraocular caliper is a modified intraocular caliper with standard calibration on the rinse needle.

Active Comparator: Verion navigation system-assisted capsulotomy group

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.

Procedure: Verion navigation system-assisted capsulotomy
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.

Outcome Measures

Primary Outcome Measures

  1. Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm) [During the surgery]

    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

  1. Uncorrected and corrected visual acuity [One month after surgery]

    Visual acuity is evaluated with ETDRS visual acuity chart.

  2. Ideal ratio of capsulorhexis [During the surgery]

    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.

  3. Grades of capsulorhexis-IOL overlap [During the surgery]

    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.

  4. Distance between pupil center and capsulorhexis center [During the surgery]

    Measured by Image J image analysis software.

  5. Horizontal and vertical diameter of capsulorhexis [During the surgery]

    Measured by Image J image analysis software.

  6. Intraocular lens tilt [One month after surgery]

    Measured by anterior segment OCT (CASIA2).

  7. Intraocular lens decentration [One month after surgery]

    Measured by anterior segment OCT (CASIA2).

  8. Intraocular aberrations [One month after surgery]

    Measured by OPD-SCAN III.

  9. Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm) [One month after surgery]

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhongshan Ophthalmic Center,Sun Yat-Sen University Guangzhou China 510060

Sponsors and Collaborators

  • Zhongshan Ophthalmic Center, Sun Yat-sen University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhongshan Ophthalmic Center, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT04977115
Other Study ID Numbers:
  • 2021KYPJ110
First Posted:
Jul 26, 2021
Last Update Posted:
Jul 26, 2021
Last Verified:
Jul 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 26, 2021