The effect of eye patching on the improvement of corneal epithelial layer and clinical symptoms in patients with UV keratitis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015092124124N1

Enrollment

Registered

2015-10-27

Start date

2015-08-22

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

Ulta violet Keratitis. Keratitis

Interventions

use drop cholobiotic and drop homatropine 2% and eye oint erythromycineyes patching in patch group

use drop cholobiotic and drop homatropine 2% and eye oint erythromycin and dont patch in group without patch.

Intervention 1: use drop cholobiotic and drop homatropine 2% and eye oint erythromycineyes patching in patch group. Intervention 2: use drop cholobiotic and drop homatropine 2% and eye oint erythromy

Treatment - Other

Eligibility

Sex/Gender

All

Age

15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: being satisified to attend the study; the resultant keratitis of UV-ray in both eyes; using no effective drugs on clinical symptoms and curing the eye epithelial layer before going to the hospital (Anestocaine, Naphazoline and …); aged 15-65 years old; ability to see through both eyes; no enternal material or any effective disease on the eye keratitis; no doctor priscription on eye bandaging or dressing. Exclusion criteria: no intention to continue to attend in the study in any of levels; not getting back after 12 hours; not following the therapeutic protocol; using the effective drugs on eye during the study due to any reason except the preacribed ones.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
The improvement of corneal epithelial layer. Timepoint: before and after intervition. Method of measurement: Examination.;Pain. Timepoint: before and after intervition. Method of measurement: Visual scale of pain.;Visual actueness. Timepoint: before and after intervition. Method of measurement: snelen chart.;Redness. Timepoint: before and after intervition. Method of measurement: observation.;Tearing. Timepoint: before and after intervition. Method of measurement: tear break up time test.	—

Measure

Time frame

The improvement of corneal epithelial layer. Timepoint: before and after intervition. Method of measurement: Examination.;Pain. Timepoint: before and after intervition. Method of measurement: Visual scale of pain.;Visual actueness. Timepoint: before and after intervition. Method of measurement: snelen chart.;Redness. Timepoint: before and after intervition. Method of measurement: observation.;Tearing. Timepoint: before and after intervition. Method of measurement: tear break up time test.

—

Secondary

Measure	Time frame
Improve epithelium. Timepoint: before and after intervition. Method of measurement: Determination Examination (mm).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Rahmaninezhad

Gonabad University of Medical Sciences

abolfazl.rahmany@gmail.com+98 51 3722 3028

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026