Clinical Long-Term Evaluation of Approved and Investigational Contact Lenses

Visual Disorders Clinical Trial

Status Completed

Clinical Trial Summary

This is a multi-site, dispensing, 4-visit, 2-arm parallel group, randomized, double-masked clinical trial using a Vistakon investigational contact lens (test) and a marketed monthly replacement contact lens (control). Each subject will be assigned randomly to either the test or control lens to evaluate the long term safety and efficacy of the investigational contact lens compared to the marketed contact lens over a period of six months of lens wear.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Vision Disorders
• Visual Disorders

• NCT number: NCT02625233
• Study type: Interventional
• Source: Johnson & Johnson Vision Care, Inc.
• Status: Completed
• Phase: N/A
• Start date: October 2015
• Completion date: February 2016