Evaluation of SYSTANE Ultra Lubricant Eye Drops

Alcon

Status: Completed

Conditions: Dry Eye

Treatments: Other: Optive; Other: SYSTANE Ultra

Study type: Interventional

Funder types: Industry

Identifiers

NCT00702377

C-07-33

Details and patient eligibility

About

To evaluate the safety and efficacy of two artificial tears in dry eye patients.

Enrollment: 109 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Documented diagnosis of dry eyes
• Must not have worn contact lenses for 1 week preceding enrollment

Exclusion criteria

• Age related

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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109 participants in 2 patient groups

SYSTANE Ultra

Experimental group

Description:

SYSTANE Ultra Lubricant Eye Drops

Treatment:

Other: SYSTANE Ultra

OPTIVE

Active Comparator group

Description:

OPTIVE Lubricant Eye Drops

Treatment:

Other: Optive