Clinical Trials Logo

Aphakia clinical trials

View clinical trials related to Aphakia.

Filter by:

NCT ID: NCT05852470 Completed - Aphakia Clinical Trials

Evaluation of Clareon Vivity/Vivity Toric

Start date: May 23, 2023
Phase: N/A
Study type: Interventional

This study seeks to generate clinical data from subjects previously implanted with the Clareon Vivity/Clareon Vivity Toric IOLs or Clareon Monofocal/Clareon Toric IOLs. This study will assess key performance endpoints to support clinical benefits with model-specific data.

NCT ID: NCT05829122 Recruiting - Aphakia Clinical Trials

Sutureless Intrascleral Intraocular Lens Fixation and Modified Iris Cerclage Pupilloplasty

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

In this study, patients with various causes of pupillary dilatation were recruited, and medical records and ophthalmology examinations, including slit-lamp examination, visual acuity, best corrected visual acuity, intraocular pressure, pupil diameter, corneal endothelial cell count, fundus examination, and photophobia score, were collected. Those who met the recruitment criteria underwent modified iris cerclage pupilloplasty. The modified iris cerclage pupilloplasty was performed by making four clear corneal incisions, suturing the iris 3-4 times consecutively between each two incisions, completing 360 degrees of iris suturing in sequence, and finally tying the knot intraocularly to complete the iris cerclage.

NCT ID: NCT05821101 Recruiting - Clinical trials for Aphakia, Postcataract

Clinical Outcomes of Clareon Vivity Intraocular Lens With Mini-Monovision Approach

Start date: April 6, 2023
Phase: N/A
Study type: Interventional

Purpose is to study the clinical outcomes of Clareon Vivity and Clareon Vivity Toric intraocular lens (IOL) implants in patients who are planning to have cataract surgery in both eyes with a mini-monovision approach.

NCT ID: NCT05799950 Enrolling by invitation - Aphakia Clinical Trials

A Real-World Evidence (RWE) Long-Term Follow-Up Study to Assess Outcomes of Alcon Monofocal Intraocular Lenses

Start date: August 28, 2023
Phase:
Study type: Observational

The purpose of this post-market clinical follow-up (PMCF) study is to describe the long-term safety and performance of AcrySof Single-Piece and AcrySof Multi-Piece monofocal intraocular lenses (IOLs).

NCT ID: NCT05796674 Completed - Astigmatism Clinical Trials

Clareon IOL Retrospective Data Collection

Start date: August 18, 2023
Phase:
Study type: Observational

The purpose of this study is to provide real world evidence (RWE) on the performance of the Clareon ultraviolet absorbing (UVA) intraocular lenses (IOLs) to support the overall body of evidence on the Clareon IOL family.

NCT ID: NCT05796453 Recruiting - Presbyopia Clinical Trials

Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix

Start date: September 19, 2023
Phase: N/A
Study type: Interventional

The purpose of this Post-Market Clinical Follow-up study is to describe the long-term safety and performance of the Clareon Vivity and Vivity Toric and Clareon PanOptix and PanOptix Toric IOLs.

NCT ID: NCT05481125 Completed - Cataract Clinical Trials

Clareon Toric vs Eyhance Toric

Start date: October 10, 2022
Phase: N/A
Study type: Interventional

The primary purpose of this study is to compare the Clareon/Clareon Toric Intraocular Lenses (IOLs) to the Eyhance/Eyhance Toric IOLs in binocular Best Corrected Distance Visual Acuity (BCDVA) at 3 months postoperative.

NCT ID: NCT05290870 Enrolling by invitation - Cataract Clinical Trials

Registry Study on Intraocular Lenses Manufactured by Teleon Surgical B.V.

Start date: February 1, 2022
Phase:
Study type: Observational

This is a retrospective, observational (Registry) study aiming to collect safety and performance data on the use of intraocular lenses (IOLs) manufactured by Teleon Surgical B.V. according to routine practice.

NCT ID: NCT05202808 Recruiting - Cataract Clinical Trials

RxSight Light Adjustable Lens and Light Delivery Device New Enrollment Study

Start date: December 3, 2021
Phase: N/A
Study type: Interventional

The primary objective of this study is to conduct a post-approval study which compares the LAL to a monofocal control IOL for safety outcomes.

NCT ID: NCT04800016 Withdrawn - Presbyopia Clinical Trials

Real-World Study of Vivity Intraocular Lenses (IOLs)

Start date: June 2021
Phase: N/A
Study type: Interventional

The primary objective of this clinical study is to assess the clinical performance of the AcrySof IQ Vivity Extended Vision IOL in a Chinese population.