Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use

Alcon

Status: Completed

Conditions: Dry Eye

Treatments: Other: Systane Lubricant eye drops

Study type: Interventional

Funder types: Industry

Identifiers

NCT00347984

05-004-09

Details and patient eligibility

About

The objective of this study was to evaluate the effect of Systane® compared to marketed artificial tears on the frequency of drop use.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects age 18 (minimum); reported history of dry eye syndrome in both eyes; TFBUT ≤ 7 seconds in at least 1 eye at Visit 1; ≥ 1+ fluorescein staining score in any region in at least 1 eye at Visit 1; desire to use an artificial tear substitute for dry eye symptoms at least 4 times per day at Visit 1 and Visit 2.

Exclusion criteria

• Age less than 18 years

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind