At a glance
ClinicalIndex Comparison RecordN/ACompleted· 68 enrolled
Drug / intervention
Icare rebound tonometry +2 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Comparative Study of Icare Rebound Tonometry With Other Tonometry Modalities in Patients Following Vitreoretinal Surgery.
In Brief
A clinical study evaluating Icare rebound tonometry, Tonopen applanation, and 1 other intervention for Intraocular Pressure. Completed, enrolled 68 participants across 1 site.
Detailed 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).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntraocular Pressure
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartOct 2012
First PostedFeb 2013
Primary CompletionSep 2014
TodayJul 2026
First PostedFeb 8, 2013
Enrollment StartOct 1, 2012
Primary CompletionSep 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 13.4 years ago
Interventions
Icare rebound tonometrydevice
Tonopen applanationdevice
Goldmann applanationdevice