Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of an Investigational Eye Drop in Dry Eye Sufferers
Primary Purpose
Dry Eye Syndrome
Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Carboxymethylcellulose sodium, glycerin and polysorbate 80
Sponsored by
About this trial
This is an interventional basic science trial for Dry Eye Syndrome
Eligibility Criteria
Inclusion Criteria:
- Mild or greater dry eye symptoms.
- Evidence of evaporative dry eye
Exclusion Criteria:
- Known allergy or sensitivity to the study product(s) or its components
- Current contact lens wearer
- Systemic or ocular allergies
- Use of systemic medication which might have ocular side effects.
- Any ocular infection.
- Use of ocular medication.
Sites / Locations
- OTG Research & Consultancy
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Investigational eye drop
Arm Description
Formulation 1: Carboxymethylcellulose sodium, glycerin and polysorbate 80 based eye drops formulated for the relief of ocular surface irritation and symptoms of dryness
Outcomes
Primary Outcome Measures
Tear Film Evaporation Rate
The rate of evaporation of the tears from the ocular surface was measured. To do so the participant was required to wear a sealed goggle over the eye, which served to isolate the air surrounding the ocular surface. The temperature and humidity were measured within the sealed goggle during closed eye and open eye situations. The evaporation from the ocular surface was calculated by taking the difference between the evaporation rate of the skin taken during the closed eye measurement and the evaporation rate taken during the open eye measurement. The rate of evaporation was measured in 10^-7 g/cm^2 /s and recorded for relative humidity of 25% to 35%.
Secondary Outcome Measures
Tear Break Up Time
The tear film break-up-time (BUT) is the time elapsed between eye opening after a blink, and the appearance of the first dark spot within the tear film when observed with a wide diffuse light source of the Tearscope. This measurement is indicative of the tear film stability. Three independent measurements were recorded in each case and the median value over the three measurements calculated. The latter value constituted the secondary endpoint used in the analysis.
Ocular Surface Disease Index Score
The OSDI is a 12-item patient-reported outcomes questionnaire designed to assess the range of ocular surface symptoms, their severity, and their impact on the patient's ability to function.
The OSDI items are scored on a 0 to 4 Likert-type scale, where 0 = None of the time, 1 = Some of the time, 2 = Half of the time, 3 = Most of the time, and 4 = All of the time. Using individual item responses, an overall OSDI score is calculated. The overall OSDI score ranges from 0 to 100, where a score of 100 corresponds to complete disability while a score of 0 corresponds to no disability.
Full Information
NCT ID
NCT01339936
First Posted
April 19, 2011
Last Updated
September 26, 2013
Sponsor
Optometric Technology Group Ltd
Collaborators
Allergan
1. Study Identification
Unique Protocol Identification Number
NCT01339936
Brief Title
Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of an Investigational Eye Drop in Dry Eye Sufferers
Study Type
Interventional
2. Study Status
Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
May 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Optometric Technology Group Ltd
Collaborators
Allergan
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main objectives of the investigation will be to assess the effect of the repeated usage of an investigational eye drop on the tear film characteristics of dry eye sufferers and demonstrate the benefit of this eye drops for dry eye sufferers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye Syndrome
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Investigational eye drop
Arm Type
Experimental
Arm Description
Formulation 1: Carboxymethylcellulose sodium, glycerin and polysorbate 80 based eye drops formulated for the relief of ocular surface irritation and symptoms of dryness
Intervention Type
Device
Intervention Name(s)
Carboxymethylcellulose sodium, glycerin and polysorbate 80
Intervention Description
1 drop in each eye three times a day for a period of 30 (± 4) days
Primary Outcome Measure Information:
Title
Tear Film Evaporation Rate
Description
The rate of evaporation of the tears from the ocular surface was measured. To do so the participant was required to wear a sealed goggle over the eye, which served to isolate the air surrounding the ocular surface. The temperature and humidity were measured within the sealed goggle during closed eye and open eye situations. The evaporation from the ocular surface was calculated by taking the difference between the evaporation rate of the skin taken during the closed eye measurement and the evaporation rate taken during the open eye measurement. The rate of evaporation was measured in 10^-7 g/cm^2 /s and recorded for relative humidity of 25% to 35%.
Time Frame
after 30 days of eyedrop usage
Secondary Outcome Measure Information:
Title
Tear Break Up Time
Description
The tear film break-up-time (BUT) is the time elapsed between eye opening after a blink, and the appearance of the first dark spot within the tear film when observed with a wide diffuse light source of the Tearscope. This measurement is indicative of the tear film stability. Three independent measurements were recorded in each case and the median value over the three measurements calculated. The latter value constituted the secondary endpoint used in the analysis.
Time Frame
after 30 days of eyedrop usage
Title
Ocular Surface Disease Index Score
Description
The OSDI is a 12-item patient-reported outcomes questionnaire designed to assess the range of ocular surface symptoms, their severity, and their impact on the patient's ability to function.
The OSDI items are scored on a 0 to 4 Likert-type scale, where 0 = None of the time, 1 = Some of the time, 2 = Half of the time, 3 = Most of the time, and 4 = All of the time. Using individual item responses, an overall OSDI score is calculated. The overall OSDI score ranges from 0 to 100, where a score of 100 corresponds to complete disability while a score of 0 corresponds to no disability.
Time Frame
after 30 days of eye drop usage
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mild or greater dry eye symptoms.
Evidence of evaporative dry eye
Exclusion Criteria:
Known allergy or sensitivity to the study product(s) or its components
Current contact lens wearer
Systemic or ocular allergies
Use of systemic medication which might have ocular side effects.
Any ocular infection.
Use of ocular medication.
Facility Information:
Facility Name
OTG Research & Consultancy
City
London
State/Province
England
ZIP/Postal Code
SW1E 6AU
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of an Investigational Eye Drop in Dry Eye Sufferers
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