Dispensing Study to Assess Visual Performance of Prototype Contact Lenses

Status Completed

Clinical Trial Summary

The aim of this study is to assess visual performance of prototype soft contact lens designs compared to commercially available contact lenses over one-week of lens wear.

Clinical Trial Description

Prospective, participant-masked, multiple arm, crossover dispensing clinical trial where participants will wear prototype (test) and commercial (control) lenses bilaterally. Participants will be stratified based on their refractive error into either presbyopic or non-presbyopic group. Each of the stratified group will have a maximum of 4 parallel arms. Up to 4 test lens designs will be assessed against the control/s in each parallel arm in a randomized cross over fashion, with a minimum 2 day washout period between the lens types. Each lens assessment will require 2 scheduled clinic attendances - a fitting visit and an evaluation visit. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02214797
Study type	Interventional
Source	Brien Holden Vision
Contact
Status	Completed
Phase	N/A
Start date	September 2014
Completion date	June 2015

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT05326607` - Pilot Clinical Investigation of Adaptative Eyeglasses for the Correction of Presbyopia	N/A
Recruiting	`NCT06060041` - IC-8 Apthera IOL New Enrollment Post Approval Study
Completed	`NCT05495971` - Extended Depth of Focus Contact Lenses for Presbyopia	N/A
Completed	`NCT05464732` - Vivity IOL: Emmetropia Compared to Monovision.	N/A
Recruiting	`NCT06045299` - Evaluation of the Efficacy and Safety of LNZ101 and LNZ100 for the Presbyopia	Phase 3
Active, not recruiting	`NCT04151550` - Safety & Efficacy of the Laser Scleral Microporation Procedure (Philippines)	N/A
Not yet recruiting	`NCT05506553` - Comparison of Aspheric Toric Intraocular Lenses for Micro-monovision	N/A
Completed	`NCT02554396` - Evaluation of the Efficacy and Safety of PRX-100 in the Treatment of Early to Moderate Presbyopia	Phase 2
Completed	`NCT02235831` - DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual Performance	N/A
Enrolling by invitation	`NCT01443585` - Clinical Evaluation of a Progressive Addition Lens (PAL)	N/A
Completed	`NCT01591499` - Clinical Evaluation of Biofinity Multifocal Compared With Air Optix Aqua Multifocal and With PureVision Multifocal	N/A
Completed	`NCT04983589` - A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyopia (Old Eye) Who Receive AGN-190584 in Both Eyes Twice Daily	Phase 3
Completed	`NCT02740010` - The Visual Performances of a Progressive Multifocal Intraocular Lens With Extended Depth of Focus
Recruiting	`NCT05796453` - Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix	N/A
Completed	`NCT02516306` - A Study to Evaluate the Safety and Efficacy of EV06 Ophthalmic Solution in Improving Vision in Subjects With Presbyopia	Phase 1/Phase 2
Completed	`NCT05359380` - The Impact of Light Conditions on the Efficacy of Multifocal Intraocular Lens Implantation in Activities of Daily Living
Not yet recruiting	`NCT04522427` - Study of Presbyopia-correcting Intraocular Lenses in Eyes With Previous Corneal Refractive Surgery	N/A
Completed	`NCT03688425` - Comparison of Clinical Outcomes POD L GF vs POD F GF in Asian Eyes	N/A
Recruiting	`NCT06053463` - Evaluation of Soft Multifocal Lenses in Presbyopic Previous Contact Lens Wearers	N/A
Completed	`NCT05069415` - Monofocal IOL Visual Outcomes When Targeting Mini Monovision	N/A