Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00399061 · ClinicalTrials.gov registry record · Phase 4

Efficacy of Optive Versus Systane Concomitant With Restasis (Cyclosporine A) for the Treatment of Dry Eye Symptoms

A Phase 4 study, sponsored by Innovative Medical.

Completed
Registry status
Phase 4
Development phase
55
Enrollment target

NCT00399061: Completed Phase 4 study, sponsored by Innovative Medical.

NCT00399061 is a Phase 4 study that has completed, run by Innovative Medical. The registered enrollment target is 55 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00399061, a Phase 4 study, has completed, sponsored by Innovative Medical.

COMPLETED
Registry status
Phase 4
Development phase
55 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the efficacy of Optive versus Systane used concomitantly with topical cyclosporine for the treatment of dry eye.

Interventions

  • DRUG Systane, Optive, Restasis

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2006-11
Est. Completion 2008-09
Phase Phase 4
Innovative Medical

44 total trials

What the finished NCT00399061 record still lists

NCT00399061 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 1 intervention - of which Systane, Optive, Restasis is the first listed.

NCT00399061 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00399061 about?

NCT00399061 is a clinical study titled "Efficacy of Optive Versus Systane Concomitant With Restasis (Cyclosporine A) for the Treatment of Dry Eye Symptoms". The purpose of this study is to evaluate the efficacy of Optive versus Systane used concomitantly with topical cyclosporine for the treatment of dry eye.

What is the current status of trial NCT00399061?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 55 participants. The study started on 2006-11. Estimated completion is 2008-09.

What interventions are being tested in trial NCT00399061?

The interventions under investigation include: Systane, Optive, Restasis (DRUG).

Who is sponsoring clinical trial NCT00399061?

This trial is sponsored by Innovative Medical, which has 44 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00399061's enrollment target sits among peer trials

55 1218th of 2000 higher than 778 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01638676 · 55 participants · Phase 1

    A Phase I/II Trial of Vemurafenib and Metformin to Melanoma Patients

  • NCT01906385 · 55 participants · Phase 1

    Maximum Tolerated Dose, Safety, and Efficacy of Rhenium Nanoliposomes in Recurrent Glioma (ReSPECT)

  • NCT03007030 · 55 participants · Phase 2

    Brentuximab Vedotin in Treating Patients With CD30+ Malignant Mesothelioma That Cannot Be Removed by Surgery

  • NCT03152058 · 55 participants · Phase 2

    IMPACT Study: IMProve Pregnancy in APS With Certolizumab Therapy

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00399061, the US trial registry maintained by the National Library of Medicine. NCT00399061 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.