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Study identifier: NCT07070843 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effects of Two Different Eye Care Practices on Eye Complications in Mechanically Ventilated Intensive Care Patients

Condition: Eye Care · Nursing Care · Intensive Care Unit  ·  Sponsor: Istanbul Saglik Bilimleri University

PhaseNA
Planned participants156
Who can joinAll sexes, 18 Days to no upper limit
Healthy volunteersNo

About this study

This study was designed as a prospective, randomized controlled experimental study aiming to compare different approaches to eye care in intensive care patients receiving mechanical ventilation. In this study, patients receiving mechanical ventilation in the intensive care unit will be randomly assigned to four groups using a simple randomization method: 1. Control Group: Standard Eye Care 2. Intervention Group 1: Eye Care with Eye Care Kit 3. Intervention Group 2: Eye Care According to Eye Care Protocol 4. Intervention Group 3: Eye Care with Both Protocol and Eye Care Kit Research Hypotheses H1: Eye care provided using a care protocol is more effective in preventing the development of complications compared to standard eye care. H2: Eye care provided using an eye care kit is more effective in preventing the development of ocular complications compared to standard eye care. H3: The combined use of an eye care kit and a care protocol is more effective in preventing the development of ocular complications compared to using the care protocol alone. H4: The use of an eye care kit is more effective in preventing the development of ocular complications compared to the use of a care protocol.

This description comes directly from the study's public registry record.

Talk to the study team

Yildiz Deniz  ·  +905387251394  ·  yildizdeniz142@gmail.com

Besey Oren  ·  +905327756206  ·  Besey.oren@sbu.edu.tr

Always discuss trial participation with your own doctor first.

Locations (1)

University of Health Sciences (Sağlık Bilimleri Üniversitesi)Istanbul, Istanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07070843