CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed
Drug / intervention
Polymethyl Methacrylate-Silicone Contact Lenses +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00000123
NCT00000123Phase 3Completed

The Berkeley Orthokeratology Study

National Eye Institute (NEI)·interventional·Posted Sep 24, 1999·Updated Sep 17, 2009

In Brief

A Phase 3 clinical trial evaluating Polymethyl Methacrylate-Silicone Contact Lenses and Polymethyl Methacrylate Contact Lenses for Astigmatism and Myopia. Completed.

Detailed Summary

To evaluate the relative efficacy of orthokeratology, primarily by assessment of changes in central corneal thickness, astigmatism, visual acuity, endothelial cell density, and corneal curvature. To evaluate the relative safety of orthokeratology, primarily by assessment of changes in central corneal thickness, astigmatism, visual acuity, endothelial cell density, induced corneal edema, and epithelial staining. To assess the duration of any orthokeratology treatment effect. To study the mechanisms by which refractive error and visual acuity changes occur, in particular the contribution that comes from changes in corneal curvature and shape. To determine whether there were any predisposing ocular factors that could be used to predict which subjects will experience changes or complications.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAstigmatism, Myopia
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
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First PostedSep 24, 1999
Enrollment StartJan 1, 1978
Study CompletionFeb 1, 1979
TodayJul 2, 2026
Posted 26.8 years ago

Interventions

Polymethyl Methacrylate-Silicone Contact Lensesdevice

Polymethyl Methacrylate Contact Lensesdevice