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Acute Comfort and Blur of Systane Ultra and Systane

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Alcon

Status

Completed

Conditions

Dry Eye

Treatments

Other: Systane Ultra Lubricant Eye Drops
Other: Systane Lubricant Eye Drops

Study type

Interventional

Funder types

Industry

Identifiers

NCT00748865
M-08-09

Details and patient eligibility

About

To evaluate drop comfort, acceptability, preference and blue profile between two marketed artificial tears in both dry eyes and non-dry eye patient population.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Documented diagnosis of dry eye

Exclusion criteria

  • Use of contact lens within 7 days preceding enrollment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

20 participants in 2 patient groups

Systane Ultra
Experimental group
Description:
Systane Ultra 1 drop each eye one time
Treatment:
Other: Systane Ultra Lubricant Eye Drops
Systane
Active Comparator group
Description:
Systane 1 drop each eye one time
Treatment:
Other: Systane Lubricant Eye Drops

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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