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NCT00622037 · ClinicalTrials.gov registry record · Phase 4

Bilateral, Masked Comparison of PEG-400 Based Artificial Tear and Systane for the Treatment of Dry Eye Signs, Symptoms and Visual Quality

A Phase 4 study, sponsored by Bp Consulting.

Completed
Registry status
Phase 4
Development phase
70
Enrollment target

NCT00622037: Completed Phase 4 study, sponsored by Bp Consulting.

NCT00622037 is a Phase 4 study that has completed, run by Bp Consulting. The registered enrollment target is 70 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00622037, a Phase 4 study, has completed, sponsored by Bp Consulting.

COMPLETED
Registry status
Phase 4
Development phase
70 participants
Enrollment target

Study Summary

To evaluate and compare the effects of PEG-400 based artificial tear and Systane tears in mild-moderate dry eye patients. TBUT, Visual impact and subjective evaluations will be assessed in this month long trial.

Interventions

  • DRUG Systane
  • DRUG PEG-400 based artificial tear

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2008-02
Est. Completion 2008-05
Phase Phase 4
Bp Consulting

10 total trials

What the finished NCT00622037 record still lists

NCT00622037 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 2 interventions - of which Systane is the first listed.

NCT00622037 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00622037 about?

NCT00622037 is a clinical study titled "Bilateral, Masked Comparison of PEG-400 Based Artificial Tear and Systane for the Treatment of Dry Eye Signs, Symptoms and Visual Quality". To evaluate and compare the effects of PEG-400 based artificial tear and Systane tears in mild-moderate dry eye patients. TBUT, Visual impact and subjective evaluations will be assessed in this month long trial.

What is the current status of trial NCT00622037?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2008-02. Estimated completion is 2008-05.

What interventions are being tested in trial NCT00622037?

The interventions under investigation include: Systane (DRUG), PEG-400 based artificial tear (DRUG).

Who is sponsoring clinical trial NCT00622037?

This trial is sponsored by Bp Consulting, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00622037's enrollment target sits among peer trials

70 1043rd of 2000 higher than 931 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

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Source: ClinicalTrials.gov NCT00622037, the US trial registry maintained by the National Library of Medicine. NCT00622037 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.