Clinical Trials Directory

Trials / Completed

CompletedNCT00763360

To Compare the Ability of DiscoVisc® OVD to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery.

To Compare the Ability of DiscoVisc® Ophthalmic Viscosurgical Device (OVD) to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
184 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
49 Years
Healthy volunteers
Not accepted

Summary

The objective of the study is to assess how DisCoVisc Ophthalmic Viscosurgical Device (OVD) compares with Healon and Amvisc Plus in the protection of corneal endothelial cells, and the ability to maintain anterior chamber space, in routine cataract surgery.

Conditions

Interventions

TypeNameDescription
DEVICEDisCoVisc®Injection of DisCoVisc® Ophthalmic Viscosurgical Device (OVD) into the anterior chamber prior to and throughout the cataract surgery procedure
DRUGHealonInjection of Healon into the anterior chamber prior to and throughout the cataract surgery procedure
DRUGAmvisc PlusInjection of Amvisc Plus into the anterior chamber prior to and throughout the cataract surgery procedure

Timeline

Start date
2008-05-01
Primary completion
2010-09-01
First posted
2008-09-30
Last updated
2012-01-24
Results posted
2012-01-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00763360. Inclusion in this directory is not an endorsement.