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
| Type | Name | Description |
|---|---|---|
| DEVICE | DisCoVisc® | Injection of DisCoVisc® Ophthalmic Viscosurgical Device (OVD) into the anterior chamber prior to and throughout the cataract surgery procedure |
| DRUG | Healon | Injection of Healon into the anterior chamber prior to and throughout the cataract surgery procedure |
| DRUG | Amvisc Plus | Injection 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.