Clinical Trials Directory

Trials / Terminated

TerminatedNCT01317030

Tear Evaluation Between Habitual Contact Lens Wearers and Non Contact Lens Wearers

Tear Evaluation Between Habitual Contact Lens Wearers and Non Contact Lens Wearers Using a Schirmer Strip for Tear Collection

Status
Terminated
Phase
Study type
Observational
Enrollment
25 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

to evaluate tears between habitual contact lens wearers and non contact lens wearers

Detailed description

The objective of this study is to evaluate tears between habitual contact lens wearers and non contact lens wearers using a Schirmer Strip for tear collection.

Conditions

Interventions

TypeNameDescription
DEVICEContact Lens WearSenofilcon A lenses will be rubbed and rinsed with Bausch + Lomb Sensitive Eyes Saline. The lenses will then be placed into Biotrue multi-purpose solution and soaked for at least 10 hours but no more than 24 hours prior to lens insertion into one eye.
DEVICEContact Lens WearSenofilcon A lenses will be rubbed and rinsed each side with Bausch + Lomb Sensitive Eyes Saline just prior to lens insertion into fellow eye.
OTHERNon-Contact Lens WearNo intervention

Timeline

Start date
2011-02-01
Primary completion
2011-03-01
Completion
2011-04-01
First posted
2011-03-17
Last updated
2020-01-09
Results posted
2020-01-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01317030. Inclusion in this directory is not an endorsement.

Tear Evaluation Between Habitual Contact Lens Wearers and Non Contact Lens Wearers (NCT01317030) · Clinical Trials Directory