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Cataract clinical trials

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NCT ID: NCT01677351 Recruiting - Pain Clinical Trials

Assessment of the Effect of Clonidine for Cataract Surgery

Start date: July 2011
Phase: Phase 2
Study type: Interventional

Clonidine, an agonist for alfa2 pre-synaptic, has been shown to be an effective adjuvant therapy for acute postoperative pain and has been shown an effect in sedative, intra-ocular and blood pressure and arrhythmias.The objective of this study is evaluating the analgesic effect of clonidine and its repercussion on arterial and intraocular pressure and arrhythmias for cataract surgery.

NCT ID: NCT01666210 Completed - Clinical trials for Ocular Inflammation and Pain

Phase II Study Evaluating Safety/Efficacy of OTX-DP for Treatment of Ocular Inflammation and Pain After Cataract Surgery

Start date: October 2012
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of OTX-DP as a sustained release drug (dexamethasone) depot when placed in the canaliculus of the eyelid for the treatment of ocular inflammation and pain in subjects who have undergone cataract extraction with intra-ocular lens implantation.

NCT ID: NCT01664819 Completed - Cataract Clinical Trials

Antioxidants for Prevention of Cataracts Follow-up Study

Start date: August 2012
Phase: N/A
Study type: Interventional

Aravind Eye Hospital and the University of California, San Francisco (UCSF) Proctor Foundation collaborated on the Antioxidants for the Prevention of Cataract Study from 1997-2002. (1) In the study, 798 participants aged 35-50 years were enrolled from 5 rural villages, and randomized to thrice weekly antioxidants (vitamin C, 500 mg; beta carotene, 15 mg; and alpha-tocopherol, 400 IU) or placebo. After 5 years of supplementation, there was no significant difference in cataract formation between the antioxidant group and placebo. In this follow-up study, we will return to study villages to determine whether rates of cataract surgery are different in the 2 groups. 1. Gritz DC, Srinivasan M, Smith SD, et al. The Antioxidants in Prevention of Cataracts Study: effects of antioxidant supplements on cataract progression in South India. The British journal of ophthalmology 2006;90:847-51.

NCT ID: NCT01659801 Completed - Cataract Clinical Trials

Evaluation of the BunnyLens TR Intraocular Lens

Start date: May 21, 2012
Phase: N/A
Study type: Interventional

With age, a human crystalline lens opacifies (cataract) disabling the eye in generating a clear, well contrasted image. The only therapeutic solution to this problem is surgical replacement of the crystalline lens with an intraocular lens (cataract surgery). In addition to the cataract, the person might suffer from pre-existing cormeal astigmatism. In cases of severe corneal astigmatism, the standard IOL might not provide the optimal result, and additional surgical procedures as Incisional Keratotomy or Limbal Relaxing Incisions might be required. BunnyLens TR IOL is an Aspheric Toric intraocular lens providing a precise, superior alternative to surgical treatment of pre-existing corneal astigmatism. The BunnyLens TR IOL is designed for micro-incision cataract surgery (MICS), through 1.8mm incisions. The aims of this study are to: - Demonstrate a reduction in refractive cylinder compared to pre-operative corneal astigmatism - Exceed monocular best corrected distance visual acuity results provided in ISO guidelines.

NCT ID: NCT01657266 Completed - Cataract Clinical Trials

Efficacy and Safety of PRO-155 Versus Nevanac in Post Phacoemulsification

Start date: December 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate efficacy and safety of the ophthalmic solution PRO-155 in patients post phacoemulsification.

NCT ID: NCT01654159 Enrolling by invitation - Cataract Clinical Trials

Assessment of Visual Function and Optics in Intraocular Lenses

Start date: September 2013
Phase: N/A
Study type: Interventional

The main objective of this research is to assess visual function and optical performance of CE marked, implanted intraocular lenses to understand the individual factors that affect their performance and how these may be improved in future designs and to evaluate measurement techniques. All outcome measures will be captured 3-6 months after surgery

NCT ID: NCT01621789 Completed - Cataract Clinical Trials

Efficacy of Lutein, Zeaxanthine and Trypan Blue to Stain the Anterior Lens Capsule

Start date: June 2012
Phase: Phase 3
Study type: Interventional

Effectiveness of lutein, zeaxanthin and trypan blue to stain the anterior lens capsule during cataract phacoemulsification.

NCT ID: NCT01615861 Completed - Cataract Clinical Trials

Evaluation of Clinical Outcomes Following Implantation of a Sub-2mm Hydrophilic MICS Intraocular Lens

Start date: November 8, 2012
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate clinical outcomes following sub-2 mm micro-incision cataract surgery (MICS) and intraocular lens (IOL) implantation. This study is evaluated in two Phases - V4 (6M) endpoint: primary analysis - V5 (12M) and V6 (34M): EPCO score and Nd Yag incidence analysis

NCT ID: NCT01605942 Terminated - Cataract Clinical Trials

A Safety and Efficacy Study of a Dexamethasone Drug Delivery System for Postoperative Inflammation and Pain After Cataract Surgery

Start date: June 2012
Phase: Phase 1
Study type: Interventional

This is a safety and efficacy study of a Dexamethasone Drug Delivery System for anterior segment inflammation and pain following cataract extraction with lens implantation.

NCT ID: NCT01605058 Not yet recruiting - Cataract Clinical Trials

Visual Performance With a Trifocal Intraocular Lens

Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the visual performance of a trifocal intraocular lens at distance, near and intermediate viewing, by way of visual acuity measurement, contrast sensitivity. Patient satisfaction and quality of vision will also be assessed by way of a questionnaire.