N/A
Completed N=68
iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery
Intraocular Pressure
Source: ClinicalTrials.gov NCT01786954 ↗
Enrolled (actual)
68
Serious AEs
0.0%
Results posted
Feb 2016
Primary outcomePrimary: Measurement of Intraocular Pressure — 15.9; 16.0; 16.9 mm Hg
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).
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Measurement of Intraocular Pressure |
15.9; 16.0; 16.9 | — |
| SECONDARY Adverse Events |
0; 0; 0 | — |
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
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. Informational only — not medical advice.