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Efficacy of FreshKote and Systane for the Treatment of Dry Eye and Improvement of Osmolarity

Primary Purpose

Dry Eye

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
FreshKote
Systane
Sponsored by
Innovative Medical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dry Eye

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Dry eye patients with Level 2 disease or greater as defined by the Delpi Panel
  • Tear osmolarity of at least 308 mosm
  • At least 18 years of age, Male or Female
  • Willing to provide written informed consent
  • Likely to complete all study visits
  • If currently using ocular lubricants, must complete a 10-14 day washout

Exclusion Criteria:

  • Presence of any active ocular disease other than dry eye
  • Use of topical ophthalmic medications
  • Use of contact lenses during the trial
  • Pregnant or nursing, or planning a pregnancy. Patients will be asked if they are pregnant or may be pregnant and excluded if they answer in the affirmative.
  • Any known sensitivity to any ingredients of either study drop
  • Oral anti-inflammatory medications, omega 3 supplements, or doxycycline
  • Punctal plugs inserted within the last 6 months or less
  • Uncontrolled systemic disease
  • Subjects with known sensitivity or inappropriate responsiveness to any of the medications used.
  • Acute or chronic disease or illness that would increase risk or confound study results (e.g., uncontrolled diabetes mellitus, immunocompromised, etc.)
  • Corneal abnormalities (e.g., ecstatic diseases, degenerations, or corneal dystrophies of the stroma or endothelium)
  • Concurrent participation or participation in the last 30 days in any other clinical trial

Sites / Locations

  • Jackson Eye, S.CRecruiting
  • Pepose Vision InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

FreshKote

Systane

Arm Description

Outcomes

Primary Outcome Measures

TBUT
Test that measures how long it takes for the tears to break up
Best Corrected Visual Acuity
Vision obtained with the best possible lens correction (glasses or contact lenses)

Secondary Outcome Measures

Full Information

First Posted
June 29, 2011
Last Updated
June 13, 2012
Sponsor
Innovative Medical
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1. Study Identification

Unique Protocol Identification Number
NCT01386073
Brief Title
Efficacy of FreshKote and Systane for the Treatment of Dry Eye and Improvement of Osmolarity
Official Title
Efficacy of FreshKote and Systane for the Treatment of Dry Eye and Improvement of Osmolarity
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
November 2012 (Anticipated)
Study Completion Date
November 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Innovative Medical

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the efficacy of FreshKote and Systane for the reduction of dry eye signs and symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FreshKote
Arm Type
Active Comparator
Arm Title
Systane
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
FreshKote
Intervention Description
Three times a day for three months
Intervention Type
Drug
Intervention Name(s)
Systane
Intervention Description
three times a day for three months
Primary Outcome Measure Information:
Title
TBUT
Description
Test that measures how long it takes for the tears to break up
Time Frame
Three months
Title
Best Corrected Visual Acuity
Description
Vision obtained with the best possible lens correction (glasses or contact lenses)
Time Frame
Three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Dry eye patients with Level 2 disease or greater as defined by the Delpi Panel Tear osmolarity of at least 308 mosm At least 18 years of age, Male or Female Willing to provide written informed consent Likely to complete all study visits If currently using ocular lubricants, must complete a 10-14 day washout Exclusion Criteria: Presence of any active ocular disease other than dry eye Use of topical ophthalmic medications Use of contact lenses during the trial Pregnant or nursing, or planning a pregnancy. Patients will be asked if they are pregnant or may be pregnant and excluded if they answer in the affirmative. Any known sensitivity to any ingredients of either study drop Oral anti-inflammatory medications, omega 3 supplements, or doxycycline Punctal plugs inserted within the last 6 months or less Uncontrolled systemic disease Subjects with known sensitivity or inappropriate responsiveness to any of the medications used. Acute or chronic disease or illness that would increase risk or confound study results (e.g., uncontrolled diabetes mellitus, immunocompromised, etc.) Corneal abnormalities (e.g., ecstatic diseases, degenerations, or corneal dystrophies of the stroma or endothelium) Concurrent participation or participation in the last 30 days in any other clinical trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jenna Piel
Phone
951-653-5566
Email
j.piel@imedsonline.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay Pepose, MD
Organizational Affiliation
Pepose Vision Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mitch Jackson, MD
Organizational Affiliation
Jackson Eye, S.C
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jackson Eye, S.C
City
Lake Villa
State/Province
Illinois
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jenna Piel
Phone
951-653-5566
Email
j.piel@imedsonline.com
First Name & Middle Initial & Last Name & Degree
Mitch Jackson, MD
Facility Name
Pepose Vision Institute
City
Chesterfield
State/Province
Missouri
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jenna Piel
Phone
951-653-5566
Email
j.piel@imedsonline.com
First Name & Middle Initial & Last Name & Degree
Jay Pepose, MD

12. IPD Sharing Statement

Learn more about this trial

Efficacy of FreshKote and Systane for the Treatment of Dry Eye and Improvement of Osmolarity

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