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iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery

NCT01786954 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2016-05-23

Study results available
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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).

Conditions

  • Intraocular Pressure

Interventions

DEVICE

Icare rebound tonometry

DEVICE

Tonopen applanation

DEVICE

Goldmann applanation

Sponsors & Collaborators

Principal Investigators

  • Paul Hahn, MD, PhD · Duke University Eye Center

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2014-09-30
Completion
2014-09-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT01786954 on ClinicalTrials.gov