Clinical Trials Directory

Trials / Unknown

UnknownNCT04122664

Posterior Capsular Opacification and Glistenings in Hydrophobic and Hydrophilic Intraocular Lenses

Prospective Randomized Controlled Study Measuring Posterior Capsular Opacification, Lens Glistenings, Tilt and Decentration, and Visual Outcomes Following Insertion of the RayOne Hydrophobic Lens 800C and the RayOne Hydrophilic Lens 600C.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
176 (estimated)
Sponsor
Guy's and St Thomas' NHS Foundation Trust · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Accepted

Summary

A prospective randomized controlled clinical study to measure posterior capsular opacification, objective measurement of glistenings and intraocular lens tilt and decentration as well as visual outcomes following insertion of a monofocal, aspheric, hydrophobic acrylic intraocular lens: the RayOne® Hydrophobic lens 800C and a monofocal aspheric, hydrophilic acrylic intraocular lens: the RayOne® Hydrophilic lens 600C

Conditions

Interventions

TypeNameDescription
DEVICERayOne® Hydrophobic lens 800CPatients will receive a monofocal, aspheric, hydrophobic acrylic intraocular lens: the RayOne® Hydrophobic lens 800C
DEVICERayOne® Hydrophilic lens 600CPatients will receive a monofocal aspheric, hydrophilic acrylic intraocular lens: the RayOne® Hydrophilic lens 600C.

Timeline

Start date
2019-10-14
Primary completion
2022-05-01
Completion
2022-05-01
First posted
2019-10-10
Last updated
2019-10-10

Source: ClinicalTrials.gov record NCT04122664. Inclusion in this directory is not an endorsement.