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Cataract clinical trials

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NCT ID: NCT03356847 Completed - Cataract Clinical Trials

Evaluation of the Rotational Stability of the Monofocal SISA Implant Following Cataract Surgery

SISALens
Start date: September 29, 2017
Phase: N/A
Study type: Interventional

A good efficacy as well as good rotary stability is expected with the ocular implant.

NCT ID: NCT03355924 Completed - Cataract Clinical Trials

DMEK And Cataract Surgery: Comparison Of Sequential Versus Combined Procedure

CISIPHE
Start date: November 1, 2016
Phase:
Study type: Observational

The aim of this study is to describe the outcomes of phaco-DMEK (Descemet Membrane Endothelial Keratoplasty ) according to a sequential versus a combined procedure

NCT ID: NCT03350503 Completed - Cataract Clinical Trials

AcrySof IQ Toric A-Code Post-Market Clinical Study

Start date: January 30, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to clinically confirm the rotational stability of a modified AcrySof IQ toric intraocular lens (IOL) in a Japanese population.

NCT ID: NCT03347981 Completed - Cataract Clinical Trials

Clinical Study to Compare Visual Performance of Two Trifocal IOLs

PHY1702
Start date: October 2, 2017
Phase: N/A
Study type: Interventional

Prospective, randomised, controlled, single-surgeon, single-center post-market clinical follow up study to compare the clinical outcomes of two trifocal IOLs with different material

NCT ID: NCT03342794 Recruiting - Congenital Cataract Clinical Trials

Morphologic and Biometric Characteristics of Preexisting Posterior Capsule Defects in Congenital Cataracts During the First Year of Life

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

Few descriptive studies have focused on the anatomical parameters in patients with preexisting PCDs. The characteristics of cataract morphology and anatomical parameters in these patients remained unclear, when compared with CC patients with intact posterior capsule. We conduct the current study to compare the cataract morphology and preoperative parameters, including central corneal thickness, axial length, anterior chamber depth, lens thickness, corneal diameter, keratometry,dialated pupil diameter and intraocular pressure, between CC patients with preexisting PCDs and those with intact posterior capsule, and to explore potential risk factors for preexisting PCDs.

NCT ID: NCT03341624 Recruiting - Congenital Cataract Clinical Trials

Congenital Cataract With Persistent Fetal Vasculature

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

To observe the clinical characteristics and surgical treatment of 24 cases of congenital cataract complicated with Persistent Fetal Vasculature (PFV) in 28 cases of congenital cataract in our hospital.

NCT ID: NCT03340389 Recruiting - Clinical trials for Age-related Cataract

Dysfunctional Lens Index Serves as a Novel Surgery Decision Maker for Age-related Cataracts

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

To study the correlations among the dysfunctional lens index (DLI), Lens Opacities Classification System III (LOCS III) nuclear opalescence grading score, preoperative corrected distance visual acuity (CDVA), the objective scatter index (OSI) and Scheimpflug based average lens density in age-related cataracts. To investigate the potential of the DLI as a novel surgery decision maker via the Operating Characteristic (ROC) curve analysis.

NCT ID: NCT03329976 Recruiting - Clinical trials for Surgery for Cataract

Validation of a Prognostic Score for Good Visual Recovery at One Year Following Combined Surgery for Cataract and Idiopathic Epiretinal Membrane

PROCATMER
Start date: April 3, 2018
Phase:
Study type: Observational

The prevalence of idiopathic epiretinal membranes (ERM) in people over 50 is estimated at 6 to 19%. Even though most cases show very few symptomats, they may induce alterations of the underlying retina and lead to visual impairment likely to greatly diminish quality of life in patients. Thanks to the ever-improving quality of vitreo-retinal surgery, ablation of these membranes is a frequent and safe procedure allowing a functional gain in the majority of cases. Given the increasing prevalence in the population concerned and the accelerated ageing of the lens after vitrectomy, cataract surgery is often associated with removal of the membrane. On the basis of a study in 142 patients, it was possible to identify clinical and morphological prognostic factors and to inclure them in a score to assess the chances of complete functional recovery at one year following the procedure . Age of the patient, the duration of symptoms, initial visual acuity and the quality of the junction between external and internal segments of photoreceptors in optic coherence tomography (OCT) appeared as significantly related to visual results. Using this score in a new prospective cohort would allow the investigators to make it a reliable and easy-to-use tool at the service of ophthalmologist surgeons and their patients and would provide scientific confirmation of the interest of earlier surgery in this disease. It would also allow the investigators to define in a validated and reproducible manner, a threshold for an ndication for ERM surgery, which is currently based on relatively subjective criteria mostly related to visual acuity.

NCT ID: NCT03324295 Recruiting - Cataract Cortical Clinical Trials

Aqueous Urea Concentration May be Related to Cataract Development

Start date: January 2017
Phase: N/A
Study type: Observational

cataracts could be cured with eye drops. Some studies reported that in chronic renal failure, the occurrence of cataract is rare and the mechanism is unknown. The aim of this research is to describe correlation between urea concentration in the serum and aqueous humor and development of age related cataract.

NCT ID: NCT03320473 Completed - Cataract Clinical Trials

IOL Implantation After KAMRA Inlay Removal

Start date: December 5, 2017
Phase: N/A
Study type: Interventional

A. The primary purpose of the study is to evaluate outcomes of aphakic eyes implanted with the IC-8 IOL following cataract removal in prior inlay patients after KAMRA inlay removal. B. The secondary purpose of the study is to determine whether there are any changes in biometry measurements before and after the inlay removal and how the changes affect the calculated IOL power.