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Cataract clinical trials

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NCT ID: NCT03247751 Completed - Cataract Clinical Trials

Evaluation of the Rotational Stability

Start date: June 2016
Phase: N/A
Study type: Interventional

To evaluate rotational stability of the investigational device implanted after cataract surgery.

NCT ID: NCT03242629 Completed - Congenital Cataract Clinical Trials

Comparison Between Oral and Enema of Chloral Hydrate

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

To compare the clinical sedative effect and safety using 10% chloral hydrate during ophthalmic examinations for oral vs enema group.The patients were randomly divided into two groups (oral group and enema group) using a computer random number generator with a 1:1 allocation (simple randomization, odd number for oral group and even number for enema group).

NCT ID: NCT03242486 Completed - Cataract Clinical Trials

Clinical Evaluation of Toric Intraocular Lens

Start date: December 2014
Phase: N/A
Study type: Interventional

Evaluate efficacy and safety of the toric IOL implanted into aphakic eye with corneal astigmatism after cataract surgery.

NCT ID: NCT03240848 Completed - Cataract Clinical Trials

Comparison of Artificial Intelligent Clinic and Normal Clinic

Start date: August 9, 2017
Phase: N/A
Study type: Interventional

In this study, the investigators provide participants≤14 years old the artificial intelligent clinic or normal clinic in the purpose of seeking out a better way to make a definite diagnosis with high efficiency and accuracy, and report a prospective, randomized controlled study aiming at comparison of artificial intelligent clinic and normal clinic for diagnosing congenital cataract.

NCT ID: NCT03224728 Completed - Cataract Clinical Trials

Spherical Aberration on the Optical of Two Different Aspherical Intraocular Lenses

Start date: September 2015
Phase: N/A
Study type: Observational [Patient Registry]

Purpose: To compare the effect of spherical aberration on optical quality in eyes with two different aspherical intraocular lenses Methods: In this prospective, randomized clinical trial 120 eyes of 60 patients underwent phacoemulsification. In patient's eyes an aberration-free aspherical IOL (Aspira-aA; Human Optics) or an aberration-correcting aspherical IOL (Tecnis ZCB00; Abott Medical Optics) were randomly implanted. Three months after surgery visual acuity, contrast sensitivity, wavefront measurements with iTrace as well as tilt and decentration measurements with Visante anterior segment OCT were performed.

NCT ID: NCT03216655 Completed - Cataract Clinical Trials

Individual vs Cohort Long Distance Advising for Mental Care for Congenital Cataract Guardians

Start date: July 11, 2017
Phase: N/A
Study type: Interventional

Nowadays, doctors put mental health at a prior place and pay more attention to the psychological problems of ill kids' parents. In our research, we try to find a new modern and efficient psychological counseling mode to improve the mentality of parents and relieve their anxiety and depression. We divide guardians of parents into two groups .One group is given the traditional follow-up by regular phone call every month. The other is in a wechat group. A doctor send the useful information about kids care and answer questions of parents at regular time every month. The self-rating anxiety scale (SAS) and self-rating depression scale (SDS) scores of parents are marked before and after the long follow up.

NCT ID: NCT03206983 Completed - Cataract Clinical Trials

Efficacy of the Canabrava/s Pupil Expansion Device in Cataract Surgery With Small Pupils: The First 30 Cases

Start date: September 2014
Phase: N/A
Study type: Interventional

To evaluate the intraoperative stability, safety and overall efficacy of the Canabrava Ring (AJL - SPAIN) when used to expand pupils with less diameter than 5 mm and pupils with sphincter synechiae.

NCT ID: NCT03192150 Completed - Clinical trials for Inflammation and Pain Associated With Cataract Surgery

2nd Study to Assess ISV-305 Compared to Vehicle for Treatment of Inflammation and Pain Associated With Cataract Surgery

ISV-305
Start date: January 3, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the ocular safety, tolerability, and efficacy of ISV-305 (Dexamethasone in DuraSite® 2) compared to Vehicle in the treatment of inflammation and pain associated with cataract surgery.

NCT ID: NCT03192137 Completed - Clinical trials for Inflammation and Pain Associated With Cataract Surgery

Study to Evaluate ISV-305 Compared to Vehicle for Treatment of Inflammation and Pain Associated With Cataract Surgery

ISV-305
Start date: January 30, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the ocular safety, tolerability, and efficacy of ISV-305 (dexamethasone in DuraSite® 2) compared with Vehicle in the treatment of inflammation and pain associated with cataract surgery.

NCT ID: NCT03184428 Completed - Clinical trials for Posterior Capsule Opacification

Posterior Capsule Opacification Following Cataract Surgery With Implantation of the MICS IOL L313

Start date: October 1, 2015
Phase:
Study type: Observational

This study collects intra- and postoperative data from the patients´charts retrospectively and evaluates retro- and prospectively the rate of posterior capsule opacification (PCO) following implantation of the intraocular lens L 313.