N/A N=68 Randomized Diagnostic

iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery

Intraocular Pressure

Bottom Line

View on ClinicalTrials.gov: NCT01786954 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Feb 2016

Primary outcome: Primary: Measurement of Intraocular Pressure — 15.9; 16.0; 16.9 mm Hg

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Icare rebound tonometry (Device); Tonopen applanation (Device); Goldmann applanation (Device)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Duke University
Primary completion: Sep 2014

Outcome Measures

Outcome	Result	p-value
PRIMARY Measurement of Intraocular Pressure	15.9; 16.0; 16.9	—
SECONDARY Adverse Events	0; 0; 0	—

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).

Eligibility Criteria

Inclusion Criteria

Duke Eye Center patients 18 years or older
capacity to give legally effective consent
scheduled to undergo vitreoretinal surgery

Exclusion Criteria

individuals unable to give consent
minors

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01786954). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.