Skip to content

Impact of 0.05% Cyclosporine A on Visual Quality in Patients with Post-refractive Surgery Dry Eye

Impact of 0.05% Cyclosporine A on Visual Quality in Patients with Post-refractive Surgery Dry Eye

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104011
Enrollment
Unknown
Registered
2025-06-10
Start date
2023-04-01
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Post-refractive Surgery Dry Eye

Interventions

treatment group:Treatment group received an instillation of 0.05% cyclosporine A eyedrops (GYZZ H20203239, Shenyang Xingqi Pharmaceutical Co Ltd.) twice a day, 20% Deproteinized Calf Blood Extract Eye
control group:20% Deproteinized Calf Blood Extract Eye Gel (Cycloome, SHENYANG XINGQI Pharmaceutical Co., China) before bedtime and 3% Diquafosol Sodium Eye Drops (Santen Pharmaceutical Co., Japan) th

Sponsors

the Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: a. Aged between 20 and 50 years, regardless of gender. b. Underwent bilateral refractive laser surgery to the cornea within 1 to 3 months prior to enrollment, and had not been diagnosed with DES prior to the procedure. c. Meet the diagnostic criteria for post-keratorefractive surgery dry eye syndrome as outlined in the 2021 Chinese Medical Association Ophthalmology Branch Cornea and Dry Eye Group's "Chinese Expert Consensus on Dry Eye Associated with Corneal Refractive Surgery (2021)".

Exclusion criteria

Exclusion criteria: Exclusion Criteria: a. Individuals with a history or current condition of severe clinical diseases in the circulatory system, endocrine system, nervous system, digestive system, respiratory system, hematology, immunology, psychiatry, or metabolic disorders, or any other condition that could interfere with the results of the study; b. Patients with active ocular infections or ongoing inflammatory therapy; c. Patients with an allergy to any of the drug components used in the study; d. Patients with permanent occlusion of the tear ducts or other anatomical abnormalities affecting tear secretion; e. Pregnant and lactating women; f. Patients with severe psychological or cognitive impairments that prevent them from understanding the study requirements or providing informed consent; g. Individuals who may not be able to complete the project for other reasons, or who the project personnel consider should not be included.

Design outcomes

Primary

MeasureTime frame
OSDI score, Ocular Surface Disease Index;pentacam;visual quality score;dry eye examination;

Countries

China

Contacts

Public ContactHan Wei

the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People’s Republic of China

hanweidr@zju.edu.cn+86 137 7745 1900

Outcome results

None listed

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