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Tears Substitutions and Their Effects on Higher Order Aberrometery

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ClinicalTrials.gov Identifier: NCT00812721
Recruitment Status : Withdrawn (PI left institution)
First Posted : December 22, 2008
Last Update Posted : April 4, 2017
Sponsor:
Information provided by (Responsible Party):
Gina Rogers, University of Iowa

Brief Summary:
Hypothesis is that tear substitutions cause blur after they are instilled. The investigators will use aberrometry as a measurement over time after a tear formulation is used and try to determine if there are any measurable change in higher order aberrations between different tear formulations and how long it takes to return to pre-instillation measurements thus providing information on duration of the tear drop. 4 commercially available "dry eye" artificial tears formulations will be used and preservative saline will act as a control. The study will be conducted on subjects that do not have clinical evidence of dry eye syndrome to focus the data on the blur effects of the tear substitutions.

Condition or disease Intervention/treatment Phase
Dry Eye Syndrome Other: Preservative Free Saline Other: Optive Other: Refresh Moderate/Severe Other: Systane Other: Systane Ultra Not Applicable

Detailed Description:

Once consent is obtained the subject will choose from available time slots. Each subject will come to the UIHC Department of Ophthalmology at designated times for approximately one hour on five different days, for a total time commitment of approximately 5 hours. Each subject will receive the same 4 artificial tear substitutes and saline, one different drop each day. One of the four tear substitutes (brands: Systane, Systane Ultra, Optive, and Refresh) will be tested on each of the days. One drop will be used each day and the protocol of each day will be the same, the only factor changing from day to day is the drop that is being evaluated. On each study day, the subject will have a pre-instillation measurement of their higher order aberrometry of each eye. One drop of the designated drop will be placed into each of the eyes. Subsequent aberrometry measurements of each eye will be taken at immediately post-instillation, 5 minutes, 30 minutes and 60 minutes post instillation. The same protocol will be followed with a saline drop and thus each patient will act as a control.

There is no long-term follow-up.


Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Supportive Care
Official Title: Tears Substitutions and Their Effects on Higher Order Aberrometery
Study Start Date : January 2009
Estimated Primary Completion Date : June 2009
Estimated Study Completion Date : July 2009

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tears
U.S. FDA Resources

Arm Intervention/treatment
Placebo Comparator: 1
Preservative Free Saline
Other: Preservative Free Saline
One drop will be instilled into each eye once
Active Comparator: 2
Optive (TM)
Other: Optive
One drop will be instilled into each eye once
Active Comparator: 3
Refresh Moderate/Severe (TM)
Other: Refresh Moderate/Severe
One drop will be instilled into each eye once
Active Comparator: 4
Systane (TM)
Other: Systane
One drop will be instilled into each eye once
Active Comparator: 5
Systane Ultra (TM)
Other: Systane Ultra
One drop will be instilled into each eye once



Primary Outcome Measures :
  1. Measurement of a subject's higher order aberrations over time is the primary outcome measure [ Time Frame: pre drop instillation, 1, 5, 15, 30, and 60 minutes post instillation ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Subjects that do not have any complaints of dry eye and confirmed by ocular surface disease index questionnaire.
  • Visually correctable to 20/20 in each eye.
  • Non contact lens wearer.
  • No history of systemic disease associated with dry eye syndromes.
  • No current use of ocular medications.
  • Adult volunteers who agree to HIPAA standards and sign informed consent.

Exclusion Criteria

  • Patients that have dry eye symptoms or slitlamp findings consistent with dry eye.
  • Have a systemic condition that is associated with dry eye syndromes.
  • Take systemic medications that have dry as a side effect
  • Currently use artificial tears.
  • Currently are using ocular medications.
  • Currently wear contact lenses.
  • Enrollment of the investigator's office staff, relatives, or members of their respective households.
  • Enrollment of more than one member of the same household.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00812721


Locations
United States, Iowa
University of Iowa Department of Ophthalmology and Visual Sciences
Iowa City, Iowa, United States, 52242
Sponsors and Collaborators
Gina Rogers
Investigators
Principal Investigator: Gina M Rogers, MD University of Iowa Department of Ophthalmology and Visual Sciences
Study Director: Christine Sindt, OD niversity of Iowa Department of Ophthalmology and Visual Sciences

Responsible Party: Gina Rogers, Principal Investigator, University of Iowa
ClinicalTrials.gov Identifier: NCT00812721     History of Changes
Other Study ID Numbers: Iowa RR 01
First Posted: December 22, 2008    Key Record Dates
Last Update Posted: April 4, 2017
Last Verified: March 2017

Keywords provided by Gina Rogers, University of Iowa:
higher order aberrations
tear blur

Additional relevant MeSH terms:
Dry Eye Syndromes
Keratoconjunctivitis Sicca
Lacrimal Apparatus Diseases
Eye Diseases
Keratoconjunctivitis
Conjunctivitis
Conjunctival Diseases
Keratitis
Corneal Diseases