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Cataract clinical trials

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NCT ID: NCT06298890 Recruiting - Cataract Clinical Trials

The Pattern of Dry Eye Disease After Cataract Surgery

Start date: March 2024
Phase:
Study type: Observational

This study is designed to explore dry eye disease (DED) pattern: ocular surface, corneal morphological changes, patients' subjective assessment of DED and their correlations with ocular surface inflammation, pain biomarkers after cataract surgery according to ocular surface lubrication with artificial tears during long-term follow-up.

NCT ID: NCT06294795 Recruiting - Astigmatism Clinical Trials

Toric Intraocular Lens Implantation in Pediatric Cataract

TILIPC
Start date: March 1, 2024
Phase: N/A
Study type: Interventional

To evaluate the visual and refractive outcomes after an intraocular lens (IOL) implantation in pediatric eyes with cataract and preexisting corneal astigmatism

NCT ID: NCT06294405 Recruiting - Lens Opacities Clinical Trials

Intraocular Lens Implant Registry Study

Start date: February 21, 2024
Phase:
Study type: Observational [Patient Registry]

The goal of this registry study is to optimize the results with intraocular lens implants used in cataract surgery.

NCT ID: NCT06277349 Completed - Cataract Clinical Trials

Multifocal-toric IOL Compared to Multifocal IOL Combined With Limbal Relaxing Incisions for Correction of Moderate Astigmatism During Cataract Surgery

Start date: March 4, 2009
Phase: N/A
Study type: Interventional

The purpose of the present study is to compare the outcome of multifocal toric intraocular lens with standard multifocal lens plus incisional surgery in patients undergoing bilateral cataract surgery.

NCT ID: NCT06266962 Completed - Cataract Clinical Trials

Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome

Start date: July 1, 2020
Phase: Phase 4
Study type: Interventional

Intraoperative Floppy Iris Syndrome (IFIS) is a potentially serious cataract surgery complication. IFIS is most commonly associated with the chronic use of tamsulosin and other alpha1-adrenergic receptor antagonists prescribed in low urinary tract symptoms. There are a number of guidelines for operative technique modifications with the aim to prevent the development of IFIS. The study focuses on two options for prophylactic strategies: the application of atropine drops and the instillation of intracameral epinephrine.

NCT ID: NCT06264830 Not yet recruiting - Cataract Clinical Trials

3D Visualization System in Highly Myopic Cataract Operation

3D-HiMCO
Start date: June 2024
Phase: N/A
Study type: Interventional

This study aims to investigate the impact of depth of field differences between the use of the 3D imaging system (NGENUITY® 3D Visualization System, Alcon, TX, USA) and conventional optical microscope in cataract surgery for highly myopic patients on intraoperative parameters and outcomes.

NCT ID: NCT06260852 Recruiting - Cataract Clinical Trials

Identification of Minimum Focal Points in Vision Curve Formation

Start date: February 1, 2024
Phase:
Study type: Observational

The primary objective of this study is to identify how many focal points and at which distances are necessary for reliable visual curve formation and area of the curve (AoC) calculation using mathematical models and comparing the results to measurements acquired from participants that underwent uncomplicated pseudophakic presbyopia surgery.

NCT ID: NCT06257914 Not yet recruiting - Cataracts Clinical Trials

Aberrometry and Straylight Measurements as an Indication for Cataract Surgery

ASICS
Start date: February 2024
Phase:
Study type: Observational

Cataracts are a clouding of the lens of the eye. Cataract surgery replaces the cloudy lens with a clear artificial lens. It is one of the leading causes of low vision worldwide. Since cataracts are mostly age-related, the number of patients with cataracts is increasing sharply due to an ageing population. The indication for cataract surgery is currently based on the visual impairment experienced by the patient, a measurement of visual acuity and the ophthalmologist's assessment of the extent to which the clouding of the lens explains the patient's symptoms. It has been said that after cataract surgery, "the world opens up to you". However, about 10% of patients actually experience worse vision after surgery. This amounts to almost a whole month of potentially unnecessary surgery. It is therefore important to develop a more objective indicator for cataract surgery. Our study focuses on measuring the optical quality of the eye before and after cataract surgery. We also ask patients before and after cataract surgery how they themselves perceive the quality of their vision. We do this with different patient-reported outcomes. We investigate whether the objective measurement of the optical quality of the eye can predict which patients will be satisfied with the cataract surgery. With this, we aim to further improve patient care and prevent unnecessary surgery.

NCT ID: NCT06250855 Not yet recruiting - Cataract Clinical Trials

Observational Prospective Clinical Investigation on Monofocal Toric Intraocular Lens

Start date: March 2024
Phase:
Study type: Observational

Evaluation, at least one-year long-term, of the clinical performance and safety of Mini Toric Ready Intraocular Lens (IOL), a monofocal toric intraocular lens.

NCT ID: NCT06250322 Recruiting - Cataracts Clinical Trials

A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens

Start date: April 10, 2024
Phase:
Study type: Observational

Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.