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Clinical Trial Summary

In intensive care patients, normal eye protection mechanisms such as tear production, blinking and keeping the eyes closed are impaired. If eye-related complications are not diagnosed and treated in time, they can cause microbial keratitis and vision loss. This study was planned as a randomized controlled experimental study to examine the effect of using an evidence-based protocol on eye care on ophthalmologic complications. Patients who meet the inclusion criteria will be randomized, and one eye of the patients will be assigned to the intervention group (experimental group) and the other to the control group. When the study reaches 40 patients, G*Power analysis will be applied and the sample size will be decided according to the result.


Clinical Trial Description

n/a


Study Design


NCT number NCT05874453
Study type Interventional
Source TC Erciyes University
Contact Özlem Ceyhan, Assoc.Prof.
Phone +903522076666
Email ozlemg@erciyes.edu.tr
Status Recruiting
Phase N/A
Start date October 15, 2023
Completion date August 15, 2024