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UnknownNCT05433259

Biometric Factors Changes Caused by Myopia Orthokeratology (OK) Lens

The Influence on Biometric Factors Changes by Different OK Lens

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Wenzhou Medical University · Academic / Other
Sex
All
Age
8 Years
Healthy volunteers
Accepted

Summary

Subjects fit with VST or CRT type lens are reviewed 1 day to 2 year after first wearing the lens. Ocular examinations were performed, including slit-lamp biomicroscope, uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), corneal topography (Medmont E300W, Medmont Pty Ltd, Melbourne, Australia), corneal refractive power (autorefractometer, KR880, Topcon, JAPAN), corneal epithelial thickness (Optical Coherence Tomography, RTVue-XR), axial length using IOL-Master 700 (Carl Zeiss Meditec AG). To investigate corneal and retina changes caused by overnight OK lens.

Conditions

Interventions

TypeNameDescription
DEVICEOvernight orthokeratologySubjects require to wear the lenses every night, with a recommended time of 6-8 hours.

Timeline

Start date
2021-09-01
Primary completion
2022-03-12
Completion
2023-11-01
First posted
2022-06-27
Last updated
2022-06-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05433259. Inclusion in this directory is not an endorsement.

Biometric Factors Changes Caused by Myopia Orthokeratology (OK) Lens (NCT05433259) · Clinical Trials Directory