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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00399230
Enrollment
Unknown
Registered
2006-11-14
Start date
Unknown
Completion date
Unknown
Last updated
2007-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry Eye

Brief summary

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

Interventions

DRUGOptive

Sponsors

Innovative Medical
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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

* · 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026