Keratopathy. H00-H06
Conditions
Interventions
Intervention 1: Intervention group: Right eye. Intervention 2: Control group: Left eye.
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Informed consent of the patient Age range from 18 to 65 years No Blindness No keratopathy at the beginning of the study with fluorescein test No head injury or trauma that may damage the eyes Patients who do not have eye diseases Admission of patients before 24 hours of hospitalization Patients with a level of consciousness of 8 and below during the treatment period The health of both eyes before hospitalization
Exclusion criteria
Exclusion criteria: Reluctance to continue the study for any reason by the patient's legal guardian Consciousness level above 8 and its fluctuation to above 8 death discharge
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevention of dry eye syndrome. Timepoint: Examination before and after intervention, intervention for 5 continuous days, 2 times a day, 5 minutes each time. Method of measurement: Grading scale of corneal changes. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohamad Azizkhani
Arak University of Medical Sciences
Outcome results
None listed