Trials / Completed
CompletedNCT03751033
Influence of DisCoVisc Ophthalmic Viscosurgical Device (OVD) on Intraoperative Aberrometry Readings
Influence of DisCoVisc OVD on Intraoperative Aberrometry Readings for Intraocular Lens (IOL) Calculations After Cataract Extraction
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Clinical Research Consultants, Inc. · Industry
- Sex
- All
- Age
- 22 Years – 95 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to develop a nomogram that correlates intraoperative, aphakic refraction measurements when the anterior chamber is pressurized with either balanced salt solution (BSS) or DisCoVisc; and to understand how suggested IOL power selection may differ.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | BSS | Intraoperative aberrometry measurements for BSS will be performed. |
| DEVICE | DiscoVisc | Intraoperative aberrometry measurements for DiscoVisc will be performed. |
Timeline
- Start date
- 2018-09-07
- Primary completion
- 2020-01-06
- Completion
- 2020-01-06
- First posted
- 2018-11-23
- Last updated
- 2020-04-21
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03751033. Inclusion in this directory is not an endorsement.