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Efficacy and Acceptability of Two Lubricant Eye Drops

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Allergan

Status and phase

Completed
Phase 4

Conditions

Dry Eye Syndromes

Treatments

Drug: Lubricating Eye Drops (blink® Tears)
Drug: Lubricant Eye Drops (Optive™)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00756678
MA-OPT-08-001

Details and patient eligibility

About

Efficacy and acceptability of two new artificial tears following two weeks of treatment in patients with dry eye. Patients will be randomized to 1 of 2 treatments for 7 days then crossover to the alternate treatment for 7 days.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or Female
  • At least 18 years of age
  • Current use of artificial tears

Exclusion criteria

  • Any uncontrolled systemic disease
  • Pregnancy or planning a pregnancy
  • Contact lens wear

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

51 participants in 2 patient groups

1
Active Comparator group
Description:
Carboxymethylcellulose and Glycerin
Treatment:
Drug: Lubricant Eye Drops (Optive™)
2
Active Comparator group
Description:
Polyethylene glycol 400
Treatment:
Drug: Lubricating Eye Drops (blink® Tears)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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