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Normal Lacritin Levels in Human Tears- Development of a New Clinical Assay

W

Walter Reed Army Medical Center

Status

Completed

Conditions

Tear Protein Lacritin in Human Tears

Treatments

Procedure: Tear Collection

Study type

Observational

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT00487643
WRAMC WU# 07-23021

Details and patient eligibility

About

Purpose: to build a library of normal tear lacritin values by collecting tears from normal adult human subjects and to develop a non-invasive clinical assay for lacritin. Such an assay will provide more sensitive indicators of eye disease for clinicians and determine if a particular therapy, such as recombinant lacritin drops, is of benefit.

Enrollment

100 estimated patients

Sex

All

Ages

21 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Military health care beneficiary between the ages of 21-55.
  2. Male or female, of any race, and at least 21 years old and not older than 55 years old at the time of tear collection.
  3. Appropriately aged individuals who report that their eyes are "normal" and who have no active eye illness as determined by principal investigator or sub-investigator.
  4. Ability and willingness to understand and provide informed consent to participate in this study.

Exclusion criteria

  1. Irritated eye reflected by patient statements or finding of "red" eye.
  2. Individuals with any infections or inflammatory ocular condition (e.g. have "pink eye" or uveitis).
  3. Individuals diagnosed with dry eye or other ocular surface condition, including but not restricted to neurotrophic keratitis, anterior basement membrane dystrophy, and recurrent corneal erosions.
  4. Individuals who are on any topical eye medications.
  5. Anyone who reports previous reaction or the possibility of an allergic reaction to 0.5% proparacaine.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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