Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DEVICE | Overnight orthokeratology | Subjects 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.