Tear Film Thickness Measured Using a Novel Technique

Dry Eye Clinical Trial

Official title:

Tear Film Thickness Measured Using a Novel Technique

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01014780
• Other study ID #: 09-10
• Status: Completed
• Phase: N/A
• First received: November 16, 2009
• Last updated: October 8, 2010
• Start date: November 2009
• Est. completion date: October 2010

Study information

• Verified date: September 2010
• Source: Southern California College of Optometry
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The aim of this investigation is to determine the thickness of the human preocular tear film using a new method based on laser speckle. This will be a preliminary study to generate "normative" tear film thickness data in normal (i.e., non dry eye) and dry eye subjects in a clinic-based population. In addition, we will examine the short term (i.e., one week) repeatability of the method in a single setting.

The patients classified as having dry eye will also have their tear film thickness measured after instillation of an artificial tear. This will potentially reveal valuable data in retention of effect measured non-invasively as in prior studies that employed a fluorescein tracer.

Description:

We will generate "normative" tear thickness data in normal (i.e., not dry) and dry eyes in human subjects. We will examine short-term repeatability of the method, and we will examine the influence on tear thickness of a viscous eyedrop instilled into the eye.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: October 2010
• Est. primary completion date: April 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

There are no requirements as to subject race, gender or occupation. If the subjects have any questions or concerns regarding any of the inclusion or exclusion criteria, they will be encouraged to ask either investigator (Dr. Paugh or Dr. Kwan) for clarification. All subjects must meet the following criteria:

1. The informed consent document must be read, signed and dated by the subject before conducting any procedures. Additionally, the informed consent document must be signed and dated by the individual obtaining consent of the subject. HIPAA authorization must also be signed and dated by the subject.

2. Adult subjects, 18 years of age and older. Criteria for the mild to severe dry eye group must include two of the three following characteristics as demonstrated at the Eligibility visit:

1. Composite symptom score of = 7 on the Schein questionnaire:

2. Sodium fluorescein (NaFl) tear break-up time = 7 seconds in either (worse) eye

3. Cumulative sodium fluorescein (NaFl) corneal staining = 4 in either (worse) eye on a 0-20 point scale (corresponds to = 3.0 on a 0-15 scale).

3. Able and willing to follow study instructions.

4. Willing to return for the repeatability visit within 7 plus or minus 2 days of the initial visit, and within the same one-half day (i.e., either in the morning or afternoon, similar to the first tear thickness visit).

5. Subjects must have best corrected visual acuity of 20/25 or better in each eye as assessed using a standard Snellen acuity chart.

6. Subjects wearing soft contacts lenses must be willing to discontinue wear for two days before each study visit.

7. Subjects using any topical drops such as artificial tears must be willing to discontinue use of such drops for two days prior to all visits, including the baseline visit.

Exclusion Criteria:

Subjects demonstrating any medical condition that may affect the results of this study SHOULD NOT be enrolled. The following are specific conditions that exclude subjects from enrollment in this study:

1. History or evidence of ocular or intraocular surgery in either eye within the past six months. LASIK and other kerato-refractive procedure patients can qualify if the most recent surgery or enhancement was 12 or more months prior.

2. History or evidence of serious ocular trauma in either eye within the past six months.

3. History of hypersensitivity to sodium fluorescein.

4. History or evidence of epithelial herpes simplex keratitis (dendritic keratitis); vaccinia, active or recent varicella, viral disease of the cornea and/or conjunctiva; chronic bacterial disease of the cornea and/or conjunctiva; mycobacterial infection of the eye; and/or fungal disease of the eye.

5. Patients requiring use of topical ocular medications such as glaucoma or allergy medications during the study period.

6. Individuals using systemic steroids, immunosuppressive agents and/or anti-cholinergics (e.g. cold and allergy medications, tricyclic antidepressants) for treatment of autoimmune connective tissue disease may not be enrolled in the study if they have not been on a stable dosing regimen for a minimum of 30 days prior to the first visit. In addition, the dosing regimen must remain stable throughout the study period, expected to be approximately one week.

7. Individuals with diabetes.

8. Ocular conditions such as conjunctival infections, or iritis.

9. Individuals wearing rigid gas permeable contact lenses or using punctal plugs.

10. Participation in an investigational drug or device study within 30 days of entering this study.

Study Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Dry Eye

Locations

Country	Name	City	State
United States	Southern California College of Optometry	Fullerton	California

Sponsors (1)

Lead Sponsor	Collaborator
Southern California College of Optometry

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tear film thickness in normal eyes		1-3 months	No
Secondary	Tear thickness change following viscous drop instillation		1-3 months	No