Corneal Biomechanical Measurements to Guide Refractive Surgery
Official title: A Study of the Clinical Applications of a Novel Corneal Biomechanical Device in Refractive Surgery
Run by Tianjin Eye Hospital · NCT07928973 · Data updated 2026-11-12
This study tests whether measurements of corneal stiffness from a steady-state device can help tailor refractive surgery for people with nearsightedness or astigmatism.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Tianjin Eye Hospital Academic / other |
| Locations | 1 site (Tianjin, Tianjin Municipality) |
| Status | Recruiting |
| Started | November 4, 2026 |
| Main results expected | November 1, 2027 |
| Study ends | October 31, 2028 |
| Registry record updated | November 10, 2026 |
| Trial ID | NCT07928973 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with myopia or astigmatism, BCVA 20/20 or better, transparent corneas, and no other eye diseases or prior ocular surgery.
✕Probably not a fit
Patients with corneal diseases, prior eye surgery, or significant anterior segment conditions may not benefit from this biomechanical assessment.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial evaluates the accuracy of corneal Young's modulus measurements (E_CID and E_Steady-State) taken by a steady-state corneal biomechanical device in patients scheduled for refractive surgery. Measurements will be compared with standard corneal assessment tools, including Pentacam and Corvis ST. The goal is to determine if these biomechanical properties can inform surgical decisions and potentially improve outcomes. Recruitment is limited to adults with myopia or myopic astigmatism and otherwise healthy corneas, excluding those with prior ocular disease or surgery. This is an interventional feasibility assessment conducted at Tianjin Eye Hospital.
Why it matters
Potential benefit: If successful, patients may receive more personalized refractive surgery planning based on their corneal biomechanics, potentially improving safety and outcomes.
How similar studies have gone: Previous work in corneal biomechanics has shown promise in characterizing corneal properties, but direct application to guiding refractive surgery planning remains exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Best corrected visual acuity (BCVA) ≥ 20/20; 2. No other eye diseases except myopia and astigmatism; 3. The cornea was transparent, and there was no cloud or pannus; Exclusion Criteria: 1. Corneal disease; 2. Ocular trauma; 3. Previous ocular surgery; 4. Any anterior segment diseases except cataract; 5. Patients were required to stop wearing soft contact lenses for at least 2 weeks and rigid contact lenses for at least 4 weeks before examination; 6. Pregnant and lactating women;
Where it's running
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Tianjin Eye Hospital
Tianjin, Tianjin Municipality, China Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.