Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-12-29

Study Completion Date

2024-10-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Comparison of the Effect of Capsular Bend on the Rotational Stability Between Two Toric Intraocular Lenses

NCT06707740

Cataract

ACTIVE_NOT_RECRUITING

Evaluation of the Rotational Stability

NCT03247751

Cataract

COMPLETED NA

Evaluation of the Rotational Stability of The AcrySof Toric Intraocular Lens in the Capsular Bag in High Myopic Subjects

NCT01351233

Cataract

COMPLETED NA

Study of Subluxation Lens Biometrics and Postoperative Intraocular Lens Stability

NCT04685122

Subluxation of Lens

UNKNOWN

Evaluate Capsular Apposition to Intraocular Lens

NCT01605812

Capsule Opacification Tissue Adhesions Aphakia - Lens Capsule Present +1 more

UNKNOWN

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Intraocular Lens Complication Phacoemulsification

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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;

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No