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Evaluation of three methods of eye care in the prevention of ocular surface diseases

A comparative survey of three methods eye care using polyethylene cover, polyethylene cover and eye drop and polyethylene cover and eye ointment, to prevent dry eye and corneal abrasion in ICU patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201506294736N8
Enrollment
172
Registered
2016-07-02
Start date
2016-07-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: corneal erosion. Condition 2: dry eye. corneal ulcer Dry eye syndrom

Interventions

Intervention 1: At the group A, a polyethylene coating is used on a daily basis for 5 days. Intervention 2: In Group B, eye drop and polyethylene coating is used. One Drop is dropped inside of the eye
Prevention
At the group A, a polyethylene coating is used on a daily basis for 5 days.
In Group B, eye drop and polyethylene coating is used. One Drop is dropped inside of the eyelid every 8 hours. polyethylene coating is then put on the eye. Coverage will be replace on a daily basis or
In group C, polyethylene coating and ophthalmic ointment are used for 5 days. Ointment is used every 8 hours at a rate of 1 cm inside the lower eyelid. polyethylene coating replaced on a daily basis.
In the control eye, routine cares such as using of antibiotic ointment, washing skin around the eye using tap water, and taping the eyelid will used.

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age over 18 years, GCS = 8, the absence of trauma to the head and face, the lack of a history of eye disease, absence of eye problems caused by diabetes, no history of hospitalization in the ICU over the past month, tracheal tube, connected to mechanical ventilation, length of stay more than 24 hours in the ICU, closing eyelids partially due to the use of neuromuscular relaxants, the negative result of Schirmer and fluorescein test. Exclusion criteria: Return of blinking reflex, extubation, the death of patient, patient transfer  to ward

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dry eye, due to reduced blinking reflex. Timepoint: At the start of intervention and then daily during 5 days. Method of measurement: Schirmer Test.;Corneal abrasion caused by dry eye. Timepoint: At the start of intervention and then daily during 5 days. Method of measurement: manually slit lamp and fluorescein test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Khatony

Kermanshah School of Nursing and Midwifery

akhatony@kums.ac.ir+98 83 3827 9496

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026