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Treatment of Ocular Discomfort in Glaucoma Patients Using Multiple Topical Medications

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Enrolling

Conditions

Glaucoma
Ocular Surface Disease

Treatments

Drug: Xiidra (Lifitegrast ophthalmic solution) 5%

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04354545
19-000843

Details and patient eligibility

About

To evaluate glaucoma patients' response to treatment with Xiidra, an FDA-approved drug for ocular surface discomfort, which will be prescribed as standard of care treatment.

Full description

To assess glaucoma patients' response to treatment with Xiidra (Lifitegrast ophthalmic solution) 5% for ocular surface discomfort caused, in part, by topical glaucoma antihypertensive medications.

Enrollment

75 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Currently using one or more topical glaucoma antihypertensives
  • Self-described symptoms of ocular surface discomfort
  • Xiidra is being prescribed as part of the subject's standard care

Exclusion criteria

  • History of glaucoma filtration surgery, history of ocular surface surgery (pterygium, conjunctivoplasty, etc.),
  • current use of topical cyclosporine
  • current use of topical steroids
  • incisional ocular surgery within 6 months

Trial design

75 participants in 1 patient group

Group 1
Description:
Xiidra (Lifitegrast ophthalmic solution) 5% applied to both eye (OU) for 12 weeks
Treatment:
Drug: Xiidra (Lifitegrast ophthalmic solution) 5%

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Benjamin B Bert, MD; Connie Zhen

Data sourced from clinicaltrials.gov

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