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Astigmatism Management With Iris-registration Guided Corneal Relaxing Incisions or Toric IOLs During Cataract Surgery

Primary Purpose

Astigmatism, Cataract

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Femtosecond laser assisted cataract surgery with astigmatism management
Sponsored by
Kenneth J Rosenthal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Astigmatism focused on measuring corneal relaxing incisions, toric IOL, iris registration, femtosecond laser-assisted cataract surgery

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients desirous of undergoing cataract surgery.
  • Pre-existing corneal astigmatism requiring either CRIs or toric IOL implantation.
  • Patients in whom iris registration link between Cassini Ambient and Catalys femtosecond laser is successful.

Exclusion Criteria:

Patients will be excluded from participating in the study due to any of the following reasons:

  • Insufficient pupil dilation to complete Catalys treatment
  • Clinically significant corneal pathology precluding reliable Cassini topographical measurement of any cause
  • Preoperative corneal astigmatism greater than 4.00 D, or astigmatism requiring both CRIs and implantation of toric intraocular lens for correction.
  • Cassini topographical measurement deemed inconsistent with historical topographies and refractive error based on clinical judgment
  • Visually significant ocular surface disease (OSD) precluding reliable measurements and/or anticipated to affect refractive stability
  • Lid position abnormalities that may affect vision
  • Moderate or severe stage glaucoma or optic nerve disease, that would interfere with assessment of or achievement of optimal BCVA
  • Visually significant macular disease

Sites / Locations

  • Kenneth J Rosenthal, MD PC

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Astigmatism correction with iris registration guided corneal relaxing incisions

Astigmatism correction with iris registration guided implantation of toric IOLs

Arm Description

This sub-group will include patients who will undergo femtosecond laser-assisted cataract surgery (Catalys) and astigmatism correction using corneal relaxing incisions and implantation of EyHance IOL. The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient.

This sub-group will include patients who will undergo femtosecond laser-assisted cataract surgery (Catalys) and astigmatism correction with the implantation of EyHance toric II IOLs. The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient.

Outcomes

Primary Outcome Measures

Mean postoperative astigmatism
Mean postoperative astigmatism

Secondary Outcome Measures

Mean monocular uncorrected distance visual acuity
Postoperative mean monocular uncorrected distance visual acuity
Mean monocular corrected distance visual acuity
Postoperative mean monocular corrected distance visual acuity

Full Information

First Posted
September 27, 2022
Last Updated
September 29, 2022
Sponsor
Kenneth J Rosenthal
Collaborators
Johnson & Johnson Surgical Vision, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05561296
Brief Title
Astigmatism Management With Iris-registration Guided Corneal Relaxing Incisions or Toric IOLs During Cataract Surgery
Official Title
Safety and Efficacy of Astigmatism Correction by Iris-registration Guided Corneal Relaxing Incisions or Toric IOL Implantation During Femtosecond Laser-assisted Cataract Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2022 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kenneth J Rosenthal
Collaborators
Johnson & Johnson Surgical Vision, Inc.

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
Most of the patients presenting for cataract surgery also have pre-existing corneal astigmatism which if left uncorrected can adversely affect visual and refractive outcomes after cataract surgery. Pre-existing astigmatism at the time of cataract surgery can be corrected by either corneal relaxing incisions or implantation of toric IOLs. While the safety and efficacy of these procedures are well established, there are various challenges associated with these techniques that surgeons need to overcome to achieve good outcomes postoperatively. The use of iris registration technology that automatically compensates for cyclotorsion has the potential to improve the alignment accuracy of CRI or toric IOLs. The Cassini Ambient and Catalys Femtosecond Laser incorporate this technology to help cataract surgeons accurately align toric IOLs on the intended axis of implantation or accurately place CRI on the intended meridian. The present study is aimed at evaluating the efficacy of astigmatism correction during femtosecond laser-assisted cataract surgery with Catalys femtosecond laser. The patients will either undergo iris registration guided CRIs or iris registration guided alignment of toric IOLs.
Detailed Description
Surgical correction of astigmatism using corneal relaxing incisions or toric IOLs have been widely adopted to correct pre-existing astigmatism in cataract surgery patients. While the safety and efficacy of these procedures are well established, there are various challenges associated with these techniques that surgeons need to overcome to achieve good outcomes postoperatively; for instance, correction of astigmatism either with corneal relaxing incisions (CRIs) or toric IOLs during cataract surgery requires appropriate pre-operative planning based on corneal curvature measurements, biometry, nomogram/IOL selection, accurate marking for the placement of CRI/implantation of toric IOL on the intended axis, intraoperative alignment, cyclotorsion compensation, and postoperative IOL rotation, etc. The Cassini Ambient and Catalys Femtosecond Laser incorporate this technology to help cataract surgeons accurately align toric IOLs on the intended axis of implantation or accurately place CRI on the intended meridian. This is expected to improve patients' visual functioning and reduce spectacle dependence postoperatively. The Cassini Ambient provides the preoperative anterior and posterior astigmatism with iris registration. The new Catalys Precision Laser System (Johnson & Johnson Vision) with cOS 6.0 software facilitates direct importation of preoperative data from the Cassini via a wireless connection or USB drive, eliminates the need for manual axis marking as it compares the pre- and intra-operative iris anatomy data and compensates for tilt and rotation so that the laser marks are perfectly aligned to the steep meridian and the target axis. Linking preoperative diagnostic information to the laser minimizes data entry and transcription errors. It also eliminates several steps in the planning process for toric IOLs and CRI, thus improving the overall accuracy of the astigmatism correction procedure and reducing chances for error.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Astigmatism, Cataract
Keywords
corneal relaxing incisions, toric IOL, iris registration, femtosecond laser-assisted cataract surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This prospective, open-label, single-center, non-randomized, interventional study will include 50 patients who will undergo femtosecond laser-assisted cataract surgery (Catalys) and astigmatism correction by either EyHance toric II IOLs or corneal relaxing incisions and implantation of EyHance IOL. The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Astigmatism correction with iris registration guided corneal relaxing incisions
Arm Type
Other
Arm Description
This sub-group will include patients who will undergo femtosecond laser-assisted cataract surgery (Catalys) and astigmatism correction using corneal relaxing incisions and implantation of EyHance IOL. The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient.
Arm Title
Astigmatism correction with iris registration guided implantation of toric IOLs
Arm Type
Other
Arm Description
This sub-group will include patients who will undergo femtosecond laser-assisted cataract surgery (Catalys) and astigmatism correction with the implantation of EyHance toric II IOLs. The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient.
Intervention Type
Procedure
Intervention Name(s)
Femtosecond laser assisted cataract surgery with astigmatism management
Intervention Description
The alignment would be guided by preoperatively obtained iris registration using Cassini Ambient. Patients will undergo femtosecond laser-assisted cataract surgery with Catalys femtosecond laser.
Primary Outcome Measure Information:
Title
Mean postoperative astigmatism
Description
Mean postoperative astigmatism
Time Frame
postoperative 3 months
Secondary Outcome Measure Information:
Title
Mean monocular uncorrected distance visual acuity
Description
Postoperative mean monocular uncorrected distance visual acuity
Time Frame
3 months postoperatively
Title
Mean monocular corrected distance visual acuity
Description
Postoperative mean monocular corrected distance visual acuity
Time Frame
3 months postoperatively
Other Pre-specified Outcome Measures:
Title
Percentage of eyes with residual refractive astigmatism within 0.5 D
Description
Frequency distribution of postoperative refractive astigmatism
Time Frame
postoperative 3 months
Title
Proportion of eyes with uncorrected distance visual acuity 20/x or better
Description
Frequency distribution of the proportion of eyes achieving postoperative uncorrected distance visual acuity 20/x or better
Time Frame
Postoperative 3 months
Title
Spherical equivalent refractive accuracy
Description
Proportion of eyes with postoperative MRSE within 0.50 and 1.00 D
Time Frame
3 months postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients desirous of undergoing cataract surgery. Pre-existing corneal astigmatism requiring either CRIs or toric IOL implantation. Patients in whom iris registration link between Cassini Ambient and Catalys femtosecond laser is successful. Exclusion Criteria: Patients will be excluded from participating in the study due to any of the following reasons: Insufficient pupil dilation to complete Catalys treatment Clinically significant corneal pathology precluding reliable Cassini topographical measurement of any cause Preoperative corneal astigmatism greater than 4.00 D, or astigmatism requiring both CRIs and implantation of toric intraocular lens for correction. Cassini topographical measurement deemed inconsistent with historical topographies and refractive error based on clinical judgment Visually significant ocular surface disease (OSD) precluding reliable measurements and/or anticipated to affect refractive stability Lid position abnormalities that may affect vision Moderate or severe stage glaucoma or optic nerve disease, that would interfere with assessment of or achievement of optimal BCVA Visually significant macular disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kenneth J Rosenthal, MD
Phone
212 517-4500
Email
research@eyesurgery.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth J Rosenthal, MD
Organizational Affiliation
Kenneth J Rosenthal, MD PC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kenneth J Rosenthal, MD PC
City
New York
State/Province
New York
ZIP/Postal Code
10128
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Danielle Kramer
Phone
212-517-4500
Email
research@eyesurgery.org
First Name & Middle Initial & Last Name & Degree
Danielle Kramer, BS
First Name & Middle Initial & Last Name & Degree
Alexandra Scherk, OD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Astigmatism Management With Iris-registration Guided Corneal Relaxing Incisions or Toric IOLs During Cataract Surgery

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