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Application of Corneal Indentation Device for comparison of Intraocular Pressure and Corneal Biomechanical Changes before and after Excimer Laser Surgery

Application of Corneal Indentation Device for comparison of Intraocular Pressure and Corneal Biomechanical Changes before and after Excimer Laser Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024818
Enrollment
Unknown
Registered
2019-07-29
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

refractive error

Interventions

Case series:Surgery

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) After informing the clinical trial plan and its advantages and disadvantages, the patient can volunteer and cooperate with the examination and undergo surgery; (2) The gender is not limited, the age is 18-40 years old, and the refractive status is stable for more than 2 years.

Exclusion criteria

Exclusion criteria: (1) Pregnant women and lactating women; (2) Those who are allergic to topical anesthetics; (3) Have organic diseases of the eye such as corneal disease, glaucoma, ocular trauma, conjunctivitis, uveitis, ocular trauma, etc.; Have a history of ocular surgery; (4) Systemic autoimmune patients; (5) Long-term oral antipsychotic drugs or patients with depression, anxiety, sleep disorders.

Design outcomes

Primary

MeasureTime frame
Corneal Modulus;

Countries

China

Contacts

Public ContactZeng Jin

Guangdong Provincial People's Hospital

syzengjin@scut.edu.cn+86 13710678633

Outcome results

None listed

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