Clinical Trials Logo
  1. Home
  2. Corneal Staining
  3. NCT02251561

Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in Japan

Corneal Staining Clinical Trial

Official title:
Clinical Evaluation of Opti-Free III Compared to Opti-Free Plus®

Clinical Trial Summary

The purpose of this study is to compare an investigational contact lens care product (FID 109182) to a commercially available contact lens product (Opti-Free Plus®) for corneal staining when used with Acuvue® Oasys® contact lenses. The contact lenses will be pre-soaked in the products for 24-48 hours prior to a 2-hour contralateral wear period.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02251561
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date May 2014
View Details
See also
  Status Clinical Trial Phase
Completed NCT01100424 - Assessment of Tear Film-Based Proteins Associated With Care Solution Induced Corneal Staining N/A
Recruiting NCT05626478 - Assessing eFficacy and Safety of DEXTENZA 0.4 mg inseRt, Following Cataract Surgery Phase 4
Recruiting NCT00381446 - Evaluation of Corneal Staining With Various Contact Lens/Solution Combinations N/A
Completed NCT01335750 - A Clinical Comparison of Marketed Lens Care Solutions With Avaira Lens Brand N/A
Completed NCT01240122 - Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Multi-Purpose Solutions N/A
Completed NCT00483795 - Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining Phase 4
Completed NCT00518700 - Comfort Evaluation of a New MPS vs. Replenish in Contact Lens Patients Phase 4