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Clinical Trials/NCT03761745
NCT03761745
Completed
Not Applicable

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Wenzhou Medical University1 site in 1 country40 target enrollmentDecember 29, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intraocular Lens Complication
Sponsor
Wenzhou Medical University
Enrollment
40
Locations
1
Primary Endpoint
Alignment of intraocular lens
Status
Completed
Last Updated
last year

Overview

Brief Summary

To evaluate the rotational stability difference among different intraocular lens. The rotational stability is evaluated by measurement of rotation of the IOL after surgery.

Registry
clinicaltrials.gov
Start Date
December 29, 2018
End Date
October 30, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

A-Yong Yu

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Wenzhou Medical University

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years
  • Patients who had received Femtosecond laser-assisted phacoemulsification surgery with IntelliAxis-L capsular mark.
  • The operation was smooth and there were no surgical complications.

Exclusion Criteria

  • Corneal and other ocular diseases (such as corneal opacity, keratitis, glaucoma, uveitis, lens dislocation or subluxation, lens capsule relaxation, retinopathy, etc.);
  • History of ocular trauma or surgery before this cataract surgery;
  • intraoperative and postoperative complications, such as posterior capsule rupture, corneal endothelium decompensation;
  • Patients with severe or unstable heart, liver, kidney, lung, endocrine (including thyroid dysfunction), blood, mental dysfunction and other diseases affect the results of this study;

Outcomes

Primary Outcomes

Alignment of intraocular lens

Time Frame: 1 month, postoperatively

The alignment of intraocular lens was evaluated by anterior segment photography

Secondary Outcomes

  • Uncorrected Visual Acuity (UCVA) at Distance(1 day, 1 week, 1 month, postoperatively)
  • Intraocular Pressure(1 day, 1 week, 1 month, postoperatively)
  • Corrected Visual Acuity (UCVA) at Distance(1 day, 1 week, 1 month, postoperatively)

Study Sites (1)

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