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Cataract Senile clinical trials

View clinical trials related to Cataract Senile.

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NCT ID: NCT06247683 Active, not recruiting - Cataract Senile Clinical Trials

Study to Confirm Safety and Performance of a New Multifocal IOL

Start date: March 13, 2023
Phase: N/A
Study type: Interventional

Prospective, non-comparative, multicenter study on medical device with 12 months follow-up.

NCT ID: NCT06196593 Completed - Cataract Senile Clinical Trials

Visual Outcomes Following Bilateral Implantation of the Vivity Toric Intraocular Lens

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The objective of this study was to evaluate the clinical and patient reported outcomes after bilateral implantation of the AcrySof™ IQ Vivity™ Toric intraocular lens.

NCT ID: NCT06165796 Completed - Cataract Senile Clinical Trials

The Effect of LASIK on the Calibration of IOL Formula Calculation: a Comparative Study

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

Direct comparison study between previous LASIK or non-LASIK cataract eyes, the performance between non-LASIK and LASIK patients were (i) Ophthalmic examinations: UDVA, CDVA and uncorrected near visual acuity (UNVA) (40cm) and (ii) Refractive prediction error: defined as difference between postoperative sphere and target refraction.

NCT ID: NCT05790993 Completed - Cataract Senile Clinical Trials

Clinical Evaluation of the Bioli IOL Delivery System (BIOLI-D)

Start date: June 20, 2022
Phase:
Study type: Observational

Cataract surgery is one of the most frequent surgeries carried out in the world. After cataract extraction an intraocular lens (IOL) is implanted in order to compensate for the crystalline lens power and correct patient's vision. In order to allow cataract extraction and IOL insertion, during the surgery a small incision is performed by the surgeon. This incision is performed using surgical knives, and a smaller incisión is associated with less postoperatory inflammation, faster corneal wound healing, and faster visual recovery. Several studies reported the importance of smaller incisions to reduce the risk of surgically induced astigmatism. In order to implant the IOL through this small incision, the IOL must be preloaded in a injector that allows introducing the IOL eficiently and consistently. The manual injector BIOLI manufactured by AST Products (model D), CE approved, is designed specifically to allow the IOL insertion safely, precisely, and controllably. Among the main characteristics of this delivery system is its design to minimize the incision size widening while inserting the IOL. The present retrospective study aims to provide more information with regards to the clinical efficacy of the BIOLI-D delivery system for the implantation of the trifocal Asqelio TFLIO130C IOL in patients submitted to cataract surgery. This will be assessed by analyzing the change in incision size after IOL implantation and the incidence of adverse events during and after the procedure.

NCT ID: NCT05750862 Active, not recruiting - Astigmatism Clinical Trials

Accuracy of Topography Guided Automatic Marking of the Intraocular Lens (IOL) -Axis

Start date: March 20, 2023
Phase: N/A
Study type: Interventional

In cataract surgery, the opaque lens is replaced by an artificial intraocular lens. The procedure also allows for correction of an refractive error such as myopia, hyperopia or astigmatism. In case of correction of an astigmatism, the axis intraocular lens has to be alligned to the axis of the corneal astigmatism. There are serveral options, the intendet position of the axis can be marked on the cornea, either manually using ink and a special caliper or with an automatic laser device. The aim of this study is to assess the accuracy of topography guided automatic marking of the intended IOL-axis in toric IOL-implantation in femtosecond laser assisted cataract surgery (FLACS)

NCT ID: NCT05578339 Completed - Cataract Senile Clinical Trials

Predicting the Lens Capsular Bag Size Using Pre-operative Biometry

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

Aim of this study is to assess whether a high-resolution scan of the crystalline lens before surgery may be helpful in predicting post-operative capsule bag diameter.

NCT ID: NCT05417633 Recruiting - Presbyopia Clinical Trials

RayOne EMV Mini-monovision - Efficiency and Safety of 3 Grades of Mini-monovision

EMV
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Aim:To determine the effectiveness and subjective satisfaction of patients with bilateral cataract surgery and implantation of intraocular lens (IOL) RayOne EMV with enhanced optic, using different degrees of mini-monovision (up to 0.74, between 0.75 -1.24 and 1.25-1.75). To compare individual groups between themselves . In particular, we would like to compare the independence of spectacle correction when looking into the distance, at medium distance and at reading distance.

NCT ID: NCT05347615 Completed - Cataract Senile Clinical Trials

Achieving Hybrid Monovision By Paring Monofocal And EDOF Lens Technology

Start date: October 10, 2019
Phase:
Study type: Observational

Modern day cataract surgery isn't just a rehabilitative procedure anymore but rather aims at improving a patient's quality of life by reducing the need for spectacles in everyday life to a minimum. One way of achieving this goal is by using different lens technologies, such as a monofocal lens paired a lens with EDOF technology, as EDOF lenses provide an enhanced depth of focus by creating a single elongated focal point. As this "mix-and-match" is well established, the aim of this study is to compare the monofocal lens cohort to the EDOF lens cohort and evaluate visual acuity and patient satisfaction.

NCT ID: NCT05303571 Withdrawn - Cataract Senile Clinical Trials

Project Bidof - Monovision by Pairing Bifocal and EDOF Lens

Bidof
Start date: March 14, 2022
Phase:
Study type: Observational

Modern day cataract surgery isn't just a rehabilitative procedure anymore but rather aims at improving a patient's quality of life by reducing the need for spectacles in everyday life to a minimum. One way of achieving this goal is by using different lens technologies, such as a mono- or bifocal lens paired a lens with EDOF technology, as EDOF lenses provide an enhanced depth of focus by creating a single elongated focal point. As this method is well established, the aim of this study is to compare the monofocal/EDOF cohort to the bifocal/EDOF cohort and evaluate visual acuity and patient satisfaction for both combinations.

NCT ID: NCT05287269 Completed - Clinical trials for Age Related Macular Degeneration

Ocular Coherence Tomography During Cataract Assessment

Start date: November 2, 2020
Phase:
Study type: Observational [Patient Registry]

Many patients will have underlying maculopathy present when undergoing cataract surgery, which are not visible on fundoscopy alone. Knowledge of this underlying pathology will allow an improved consenting process and discussion with the patient regarding the risks, visual prognosis and recovery following cataract surgery. Incidental findings in the fellow eye would also allow for improved diagnosis and management of these patients without adding significant additional time to specialist high volume cataract assessment clinics.