Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01706237

Visual Outcomes And Contrast Sensitivity After Myopic Wavefront-Optimized Lasik With Nexisvision Shield Or Bandage Contact Lens

Evaluation Of Visual Outcomes And Contrast Sensitivity After Myopic Wavefront-Optimized Lasik With Nexisvision Shield Or Bandage Contact Lens

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Durrie Vision · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Evaluate visual outcomes and contrast sensitivity for subjects undergoing bilateral myopic LASIK with a Nexisvision Shield or bandage contact lens placed postoperatively. Early speed of visual recovery results indicate that the visual recovery in the first 4 hours after the LASIK procedure show the most variability. A patient's ability to drive after their LASIK procedure would potentially alleviate a challenge that patients often face in taking additional time off work or simply finding a ride to there LASIK procedure.

Detailed description

Laser in situ keratomileusis (LASIK) surgery has been performed worldwide since 1990. Historically, LASIK has been reported to decrease contrast sensitivity post operatively and patients have been advised to take the day off of work and potentially the day after LASIK. More recently, utilizing advanced laser technology for optimized corneal ablation and creation of the flap has the potential for improved LASIK surgery results and improved recovery time. Visual recovery and management of immediate post operative visual acuity is important for patient satisfaction.

Conditions

Interventions

TypeNameDescription
DEVICENexisvision shieldA shield is placed on the eye after LASIK. The shield is similar to a contact lens.

Timeline

Start date
2012-05-01
Primary completion
2014-06-01
First posted
2012-10-15
Last updated
2014-06-04

Source: ClinicalTrials.gov record NCT01706237. Inclusion in this directory is not an endorsement.