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NCT00198549 · ClinicalTrials.gov registry record · Phase 4

Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics

A Phase 4 study, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 4
Development phase
40
Enrollment target

NCT00198549: Completed Phase 4 study, sponsored by Bausch & Lomb Incorporated.

NCT00198549 is a Phase 4 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 40 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00198549, a Phase 4 study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 4
Development phase
40 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate Vitrase as an adjuvant to increase absorption and dispersion of other injected anesthetics

Interventions

  • DRUG Vitrase (ovine hyaluronidase) Lyophilized

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2004-09
Est. Completion 2005-03
Phase Phase 4
Bausch & Lomb Incorporated

174 total trials

What the finished NCT00198549 record still lists

NCT00198549 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Vitrase (ovine hyaluronidase) Lyophilized is the first listed.

NCT00198549 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00198549 about?

NCT00198549 is a clinical study titled "Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics". The purpose of this study is to evaluate Vitrase as an adjuvant to increase absorption and dispersion of other injected anesthetics

What is the current status of trial NCT00198549?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2004-09. Estimated completion is 2005-03.

What interventions are being tested in trial NCT00198549?

The interventions under investigation include: Vitrase (ovine hyaluronidase) Lyophilized (DRUG).

Who is sponsoring clinical trial NCT00198549?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00198549's enrollment target sits among peer trials

40 1397th of 2000 higher than 533 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 NCT00198549, the US trial registry maintained by the National Library of Medicine. NCT00198549 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.