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CompletedNCT00399230Updated Aug 21, 2007

A Comparison of Optive in Patients Previously Using Systane for the Treatment of Dry Eye

A Phase 4 interventional study of Optive in Dry Eye, sponsored by Innovative Medical. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2007-08-21.

Sponsored by Innovative Medical · Phase 4 and Interventional

Phase
Phase 4
Study type
Interventional
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

To evaluate the effectiveness of NGT (Optive) vs. Systane Tears for patients with moderate to severe dry eye disease.

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.

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

Inclusion criteria

    • Dry eye disease diagnosis

      • Patients must currently be using Systane tears at least once a day and for at least 1 month.
      • Normal lid position and closure
      • Male or female of legal age of consent
      • Informed consent has been obtained
      • Likely to complete all required follow-up visits

Exclusion criteria

Exclusion Criteria:

    • Concurrent enrollment in an investigational drug or device study, or participation in such a study within 30 days of entry into this study.

      • Subject has a condition, or is in a situation which, in the investigator's opinion, may put the subject at a significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study.
05

Study design

Phase
Phase 4
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)

Interventions

  • DrugOptive
06

Study locations

1 site
  • Dr. Rajpal
    McLean, Virginia 22102, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00399230
Lead sponsor
Innovative Medical
First posted
Nov 14, 2006
Last update
Aug 21, 2007

Study contacts

Rajesh Rajpal, MD
principal investigator · See Clearly Vision Group
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2007. You cannot join it, but the record below documents what was studied.

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