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OpenTrials
Completed

NCT Number: NCT01176045

TearLab Refractive Surgery Dry Eye Study

The primary objective of this study is to determine how pre & post-operative tear osmolarity levels relate to rates of dry eye symptoms related to refractive surgery and if differences exist in patients who are pre-treated with ocular lubricants vs. those treated only post-operatively.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Connecticut TLC, Fairfield, Connecticut, United States

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About this study

Dry eye disease is a common and major source of disability, whether occurring as a primary disorder or as a component of other diseases and its onset may be triggered or modified by exposure to systemic drugs, contact lens wear, ocular surgery and adverse environmental and work conditions. The development of a reliable, highly sensitive and specific test for the clinical diagnosis of dry eye is a major unmet clinical need, particularly to differentiate it from common conditions such as ocular allergy which exhibit similar presenting symptoms. Tear hyper-osmolarity is central to the dry eye disease process and the measurement of tear osmolarity could serve not only as a highly accurate diagnostic test but also as a measure of disease severity and a means to monitor treatment efficacy.

Recently, there have been reports in the literature regarding dry eye disease; both early and chronic following refractive surgery, with many cases potentially being previously inadvertently undiagnosed dry eye disease.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female, twenty-one years of age or older.
  • Confirmed diagnosis of refractive error receiving LASIK surgery.
  • Patient motivation and willingness to cooperate with the investigator and ability to return for all visits during the study.

Exclusion criteria

  • Compromised cognitive ability that may be expected to interfere with study compliance.
  • Clinically significant eyelid deformity or eyelid movement disorder that is caused by conditions such as notch deformity, incomplete lid closure, entropion, ectropion, hordeola or chalazia.
  • Previous ocular disease leaving sequelae or requiring current topical eye therapy other than for DED, including, but not limited to: active corneal or conjunctival infection of the eye and ocular surface scarring.
  • Active ocular allergy
  • Patients requiring punctual occlusion prior to surgery
  • Patients requiring cyclosporine ophthalmic emulsion prior to surgery
  • Standard exclusion criteria for refractive surgery used by each surgeon.
  • Known hypersensitivity to any of the agents used in testing
  • Ophthalmologic drop use within 2 hours of any visit

Treatment and study plan

Primary outcomes

  1. Relation of pre & post-operative tear osmolarity levels to dry eye and dry eye symptoms in refractive surgery

    Time frame: 6 months post surgery

Secondary outcomes

  1. To determine if differences exist in patients who are pre-treated with ocular lubricants vs. those treated only post-operatively

    Time frame: 6 months post-surgical

  2. To determine if tear osmolarity levels relate to visual acuity outcomes related to refractive surgery

    Time frame: 6 months post-surgical

Sponsors and collaborators

Lead sponsor

TearLab Corporation

Industry

Collaborators

  • Abbott Medical Optics
  • TLC Laser Eye Center

Registry information

Official study title

Measurement of Refractive Surgery Induced Dry Eye Using Tear Osmolarity Testing

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Aug 5, 2010
Registry last updated
Feb 4, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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