A Randomized Study of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract Patients With Corneal Limbus Opacity

Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04977102
Collaborator
(none)
74
1
2
15
4.9

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 for age-related cataract patients with corneal limbus opacity.

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. Too large or too small capsulorhexis can increase the incidence of intraoperative and postoperative complications.

In recent years, the image projection device Verion navigation system has been reported that it can improve the repeatability and accuracy of capsulorhexis via projecting a pre-set size ring to guide capsulorhexis. However, we found that for the patients with corneal geriatric ring, pterygium or limbal lesions leading to unclear limbal boundary, the projected capsulorhexis will deviate from the center, resulting in capsulorhexis is off center in clinical practice. Our self-developed intraocular caliper, which is modified on the conventional intraocular irrigation needle, can accurately measure the size of capsulorhexis, and mark the position and boundary of capsulorhexis on the lens anterior capsule to guide capsulorhexis, thus significantly improves the accuracy and centricity of capsulorhexis.

The purpose of this study is to compare the centricity and accuracy of intraocular caliper-assisted capsulorhexis in phacoemulsification for age-related cataract patients with corneal limbus opacity with that of Verion projection navigation system.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
74 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
A Randomized Controlled Trial Comparing Intraocular Caliper-assisted Capsulotomy Versus Verion Navigation System-assisted Capsulotomy for Age-related Cataract With Corneal Limbus Opacity
Anticipated Study Start Date :
Aug 1, 2021
Anticipated Primary Completion Date :
Jul 31, 2022
Anticipated Study Completion Date :
Oct 31, 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. Distance between pupil center and capsulorhexis center [During the surgery]

    The primary outcome was the distance between pupil center and capsulorhexis center. Clear images of the edges of IOL and capsulorhexis were taken at the end of the operation, and Image J image analysis software is used to measure the distance between pupil center and capsulorhexis center with the diameter of IOL optical surface (6 mm) as the reference by two independently professional graders at the meantime.

Secondary Outcome Measures

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

    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 was graded as 360-degree continuous overlap, 270~360-degree overlap, 180~270-degree overlap, 90~180-degree overlap, and < 90-degree overlap.

  4. Deviation of horizontal and vertical diameter of capsulorhexis from the target diameter (5.3 mm) [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. Distance between pupil center and capsulorhexis center [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 with pterygium, Corneal geriatric ring, and corneal limbus opacity;

  • 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:
NCT04977102
Other Study ID Numbers:
  • 2021KYPJ111
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