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Influence of DisCoVisc Ophthalmic Viscosurgical Device (OVD) on Intraoperative Aberrometry Readings

NCT03751033 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2020-04-21

No results posted yet for this study

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

  • Cataract

Interventions

DEVICE

BSS

Intraoperative aberrometry measurements for BSS will be performed.

DEVICE

DiscoVisc

Intraoperative aberrometry measurements for DiscoVisc will be performed.

Sponsors & Collaborators

  • Clinical Research Consultants, Inc.

    lead INDUSTRY

Principal Investigators

  • Nicole Fram, MD · Advanced Vision Care

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-07
Primary Completion
2020-01-06
Completion
2020-01-06
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03751033 on ClinicalTrials.gov