The Effect of Vitamin A Paimitate Eye Gel on Corneal Abrasions During General Anesthesia

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100052140

Enrollment

Unknown

Registered

2021-10-20

Start date

2021-11-01

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

corneal abrasions

Interventions

Experimental group:eyelid taping combined with Vitamin A Paimitate Eye Gel

Control group:eyelid taping

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Non-ocular surgery patients with general anesthesia longer than 2 hours in a reclining position, whose disinfection scope does not involve eye circumference; 2.Patients who voluntarily participate in this study can cooperate with the entire study process.

Exclusion criteria

Exclusion criteria: 1.Patients who had active ocular infection or inflammation; 2.Patients whose pre-operation CFS score are more than 3 points; 3.Patients who had ocular diseases affecting the secondary outcome; 4.Patients whose Robertson Score are less than 4 points; 5.Patients allergic to this drug or eyelid taping.

Design outcomes

Primary

Measure	Time frame
Corneal Fluorescein Staining;	—

Secondary

Measure	Time frame
Schirmer I test;Fluorescein breakup time;Conjunctiva congestion score;	—

Countries

China

Contacts

Public ContactJie Ying

Beijing Tongren Hospital

jie_yingcn@aliyun.com+86 13693572296

Outcome results

None listed

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