CClinicalTrials.gg
Status unknownNCT01386073Updated Jun 14, 2012

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

A Phase 4 interventional study of FreshKote and Systane in Dry Eye, sponsored by Innovative Medical. Status unknown at 2 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-06-14.

Sponsored by Innovative Medical · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2012), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

03

In context

Dry Eye Syndromes

1,292 studies on the registry are indexed under Dry Eye Syndromes; 191 are open to participants now.

This study's planned enrollment of 40 is below the median of 60 across 1,077 interventional studies indexed under Dry Eye Syndromes.

Browse Dry Eye Syndromes studies →

Lead sponsor

Innovative Medical is the lead sponsor of 50 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    FreshKote

    Drug: FreshKote

  • Placebo comparator
    Systane

    Drug: Systane

Interventions

  • DrugFreshKote

    Three times a day for three months

  • DrugSystane

    three times a day for three months

06

What researchers measure

Primary outcomes

  1. TBUT

    Test that measures how long it takes for the tears to break up

    Time frame: Three months

  2. Best Corrected Visual Acuity

    Vision obtained with the best possible lens correction (glasses or contact lenses)

    Time frame: Three months

07

Study locations

2 of 2 sites recruiting
  • Jackson Eye, S.C
    Lake Villa, Illinois, United States
    Recruiting
  • Pepose Vision Institute
    Chesterfield, Missouri, United States
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 14, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01386073
Lead sponsor
Innovative Medical
First posted
Jun 30, 2011
Start date
Jul 2011
Primary completion
Nov 2012 (estimated)
Completion
Nov 2012 (estimated)
Last update
Jun 14, 2012

Study contacts

Jenna Piel
Contact
j.piel@imedsonline.com
951-653-5566
Jay Pepose, MD
principal investigator · Pepose Vision Institute
Mitch Jackson, MD
principal investigator · Jackson Eye, S.C

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2012. You cannot join it, but the record below documents what was studied.

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