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The Role of Corneal Densitometry and Tear Cytokine Profiling in Personalizing Post-FS-LASIK Pharmacotherapy

The Role of Corneal Densitometry and Tear Cytokine Profiling in Personalizing Post-FS-LASIK Pharmacotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114387
Enrollment
Unknown
Registered
2025-12-11
Start date
2025-12-31
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Corneal Healing after Refractive Surgery

Interventions

Fluorometholone group:Treatment was initiated on the first postoperative day with 0.1% Fluorometholone eye drops and 0.3% Tobramycin eye drops. Both medications were administered as one drop four time
Tobramycin and Dexamethasone group:Tobramycin and Dexamethasone eye drops were administered as one drop, four times daily. The medication was discontinued after one week of use.

Sponsors

Zigong First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 40 years. (2) A preoperative spherical equivalent refraction between -10.0 D and -1.0 D. (3) Stable refraction for at least one year, with a change of = 470 µm, with an estimated residual stromal bed thickness of >= 280 µm postoperatively.

Exclusion criteria

Exclusion criteria: (1) Patients with impaired vital organ function, severe life-threatening systemic diseases, or psychiatric disorders. (2) Patients with autoimmune diseases (e.g., rheumatoid arthritis, hyperthyroidism) or diabetes mellitus. (3) Pregnant or lactating patients. (4) Patients with unstable refraction, a history of corneal trauma, or prior ocular surgery. (5) Patients with other ocular comorbidities, such as keratoconus, glaucoma, keratitis, retinal vasculitis, uveitis, or dry eye disease. (6) Patients with any systemic or local infectious disease within the past 3 months. (7) Individuals currently participating in other drug clinical trials, or those deemed by the investigator as unsuitable for the trial. (8) Patients who develop postoperative complications requiring additional ophthalmic medications. (9) Subjects with poor compliance, inability to complete the treatment and follow-up as planned, or those who voluntarily withdraw from the study.

Design outcomes

Primary

MeasureTime frame
Corneal Densitometry;

Secondary

MeasureTime frame
Tear Inflammatory Cytokines;Quality of Vision;

Countries

China

Contacts

Public ContactJun Zheng

Zigong First People's Hospital

15908265367@163.com+86 159 0826 5367

Outcome results

None listed

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