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Active clinical trials for "Aphakia"

Results 41-50 of 55

Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)

Aphakia

The purpose of this study is to evaluate the safety and effectiveness of an investigational IOL.

Completed14 enrollment criteria

Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL) With an Improved Injector System...

Aphakia

The purpose of this study is to evaluate the clinical outcomes of an investigational IOL in patients undergoing cataract extraction and intraocular lens implantation using an improved injector system.

Completed14 enrollment criteria

Evaluating Safety and Efficacy of a Modified Technique of Scleral Fixation Intraocular Lens Implantation...

AphakiaCataract

Cataract is the leading cause of blindness globally and cataract surgery with the implantation of intraocular lens (IOL) is the most commonly performed operation worldwide. After removal of the cataract, an IOL is usually implanted within the capsular bag. However, endocapsular implantation of IOL is not always feasible due to inadequate zonular or capsular support, intraoperative posterior capsule rupture, or in primary intracapsular cataract extraction. Predisposing factors including prior ocular trauma, intravitreal injection or intraocular surgery, co-existing ocular comorbidities like chronic uveitis, pseudoexfoliation syndrome, may increase the risk of failure of in-the-bag implantation. In such situation, the surgeons may consider implanting the IOL in the anterior chamber, ciliary sulcus, or using fixation techniques. In Asian eyes, the anterior chambers are often shallow and placement in anterior chamber may accelerate corneal endothelial cell loss leading to corneal decompensation, or worsen pre-existing glaucoma. Placement in the ciliary sulcus depends on the amount and integrity of the capsular remnant, and inadequate support may result in dislocation of the IOL. In recent years, newer forms of scleral fixation of IOL using glue or glue-less approach, although these procedure appeared to be simpler, the long-term stability of these IOL have not been evaluated against conventional approach with suture fixation. The main limitations of suture fixation technique are related to the sutures either intraoperatively (e.g. entanglement, failure to rotate and bury the suture knot) or postoperatively (breakage, dissolution of suture with time), and the learning curve required for surgeons in training. Our study aims to study the efficacy and safety of a modified technique of scleral fixation of an intraocular lens in the posterior chamber.

Unknown status8 enrollment criteria

Accuracy of Holladay 2 Formula in the Absence of Lens Thickness

Cataracts

Hypothesis: Holladay 2 formula is still accurate even used without lens thickness data.

Completed3 enrollment criteria

Exploratory Clinical Study for Techniques Associated With the Fluid Accommodating IOL

AphakiaPresbyopia

The purpose of this clinical study is to assess the repeatability of objective refraction using auto refraction on subjects bilaterally implanted (implanted in both eyes) with the Fluid Accommodating IOL (FAIOL).

Completed18 enrollment criteria

Comparative Study of the Optical Biometer for Measurements of the Eye

Normal Non-fluencyCataract2 more

The primary purpose of this comparative clinical study is to collect clinical data to demonstrate the equivalence of the investigational device to the predicate device for measurements of the eye. The secondary purpose is to evaluate any adverse events that occur during the clinical study.

Completed13 enrollment criteria

Intraocular Position of Secondary Iris-Fixated IOLs in Aphakic Eyes

Aphakia

The purpose of this study is to evaluate the intraocular stability and safety of secondary iris-fixated IOLs in aphakic patients.

Completed2 enrollment criteria

A Multi Focal Visual Outcome Study Using Different Near Additions

CataractAphakia

A multi-centre non-randomized clinical investigation to assess multifocal visual outcomes using different near additions, for the treatment of aphakia after cataract removal.

Terminated21 enrollment criteria

Clinical Evaluation of the Lenstec Softec HP1 Intraocular Lens

Aphakia

The study is designed as a post market evaluation of the Softec HP1 IOL for continuance of the CE certificate. The primary effectiveness endpoint is to evaluate the safety and performance levels produced by this IOL in patients requiring standard cataract surgery. There will be no change from standard procedure, other than 1 extra post op evaluation.

Unknown status33 enrollment criteria

Clareon IOL Retrospective Data Collection

AphakiaAstigmatism

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.

Completed4 enrollment criteria
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