Clinical Trials Directory

Trials / Completed

CompletedNCT01786954

iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery

A Comparative Study of Icare Rebound Tonometry With Other Tonometry Modalities in Patients Following Vitreoretinal Surgery.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
68 (actual)
Sponsor
Duke University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to compare the measurement of pressure inside the eye using three different FDA-approved devices (Icare, Tonopen, and Goldmann applanation).

Detailed description

The three above devices will be used to measure intraocular pressure in patients one day following vitreoretinal surgery. The underlying reason for surgery is not being considered in this study. The measured pressures will be compared across devices in eyes filled with fluid, gas, and silicone oil.

Conditions

Interventions

TypeNameDescription
DEVICEIcare rebound tonometry
DEVICETonopen applanation
DEVICEGoldmann applanation

Timeline

Start date
2012-10-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2013-02-08
Last updated
2016-05-23
Results posted
2016-02-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01786954. Inclusion in this directory is not an endorsement.