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Clinical Trials in China / NCT06993077
Active, not recruiting Observational

Impact of Ultraviolet Radiation and Environmental Factors on Human Ocular Biomechanics

NCT06993077 · tracked via the Priya Life Science China tracker
Sponsor
Tianjin Eye Hospital
Phase
Observational
Started
2025-01-01
Last updated
2025-05-28

Condition(s) studied

Myopia

Investigational drug(s) / intervention(s)

environment Exposure

environment Exposure: No special intervention

Study summary

This observational study aims to explore whether ultraviolet (UV) radiation and other environmental factors are associated with ocular biomechanical properties in healthy volunteers aged 18-44 years without ocular diseases, ocular surgery history, or systemic diseases.

The main questions it aims to answer are:

Is there a significant correlation between UV radiation levels and corneal biomechanical parameters?

Do environmental factors such as geographic region and seasonal variation affect corneal biomechanical behavior?

Researchers will compare ocular biomechanical parameters among populations from different geographic regions with varying levels of UV radiation to determine whether there are statistically significant correlations or differences.

Participants will:

Undergo standardized ophthalmic examinations, including visual acuity, intraocular pressure, slit-lamp evaluation, axial length, and corneal topography;

Receive corneal biomechanical assessments using the Corvis ST device;

Provide basic demographic information and medical history;

Have all data de-identified, with the study strictly following ethical approval and privacy protection protocols.

Eligibility

Sex
ALL
Min age
18 Years
Max age
44 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Inclusion Criteria Age between 18 and 44 years (based on WHO criteria); Spherical equivalent refraction (SER) ≤ 6.00 diopters; No other ocular diseases; No systemic diseases (e.g., diabetes, hypertension, cardiovascular diseases); No severe psychiatric or psychological disorders; No history of ocular surgery. Exclusion Criteria Severe psychiatric disorders; Individuals diagnosed with keratoconus, suspected keratoconus, or subclinical keratoconus (based on the Global Consensus on Keratoconus Diagnosis); Presence of other ocular diseases (e.g., glaucoma, corneal opacity, uveitis); History of intraocular or ocular surface surgeries; Presence of nystagmus or inability to cooperate with examinations; History of intraocular surgery; Presence of systemic diseases (e.g., diabetes, hypertension, cardiovascular diseases). Exclusion Criteria: * Severe psychiatric disorders; Individuals diagnosed with keratoconus, suspected keratoconus, or subclinical keratoconus (based on the Global Consensus on Keratoconus Diagnosis); Presence of other ocular diseases (e.g., glaucoma, corneal opacity, uveitis); History of intraocular or ocular surface surgeries; Presence of nystagmus or inability to cooperate with examinations; History of intraocular surgery; Presence of systemic diseases (e.g., diabetes, hypertension, cardiovascular diseases).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tianjin Eye Hospital China Tianjin Municipality

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06993077 on ClinicalTrials.gov ↗ ← All trials in China