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Comparison of intraocular pressure measurements after LASIK and SMILE refractive surgery

Comparison of intraocular pressure measurements after LASIK and SMILE refractive surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067326
Enrollment
Unknown
Registered
2023-01-04
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Ametropia

Interventions

Group 2:
Group 1:

Sponsors

Huangshi Aier Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.18-40 years old; 2. Diopter: -1.00D to -7.00D; 3. Diopter range of astigmatism: less than -6.00D; 4. The diopter has been stable for more than 2 years (the change in the past two years is less than or equal to 0.5D); 5. Stop using soft contact lenses for more than one week or stop using hard contact lenses for more than one month before the study; 6. The preoperative intraocular pressure measured by three kinds of tonometers are all in the range of 10-21 mmHg; 7. Corneal morphology is normal, without keratoconus; 8. No other eye diseases, such as cataract, glaucoma or fundus disease; 9. No eye inflammation and trauma history; 10. No history of connective tissue disease, systemic disease or drug allergy.

Exclusion criteria

Exclusion criteria: Patients with early postoperative high intraocular pressure.

Design outcomes

Primary

MeasureTime frame
ntraocular pressure;

Countries

China

Contacts

Public ContactWu Xiang

Huangshi Aier Eye Hospital

82881579@qq.com+86 15072045631

Outcome results

None listed

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