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NCT00552695 · ClinicalTrials.gov registry record · Phase 2
Lidocaine Patches Prior to Intravenous Insertion
A Phase 2 study, sponsored by Stony Brook University.
- Completed
- Registry status
- Phase 2
- Development phase
- 45
- Enrollment target
NCT00552695: Completed Phase 2 study, sponsored by Stony Brook University.
NCT00552695 is a Phase 2 study that has completed, run by Stony Brook University. The registered enrollment target is 45 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00552695, a Phase 2 study, has completed, sponsored by Stony Brook University.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 45 participants
- Enrollment target
Study Summary
This study will determine whether application of a patch containing a topical anesthetic (numbing medicine) named lidocaine can reduce the pain of subsequent insertion of an intravenous catheter in Emergency Department patients.
Primary Outcome
Pain on 100 mm Visual Aanalog Scale from 0 (no pain) to 100 (most pain).
Interventions
- DEVICE Placebo
- DEVICE Lidocaine tetracaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2007-08 |
| Est. Completion | 2008-01 |
| Phase | Phase 2 |
What the finished NCT00552695 record still lists
NCT00552695 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00552695 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00552695 about?
NCT00552695 is a clinical study titled "Lidocaine Patches Prior to Intravenous Insertion". This study will determine whether application of a patch containing a topical anesthetic (numbing medicine) named lidocaine can reduce the pain of subsequent insertion of an intravenous catheter in Emergency Department patients.
What is the current status of trial NCT00552695?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2007-08. Estimated completion is 2008-01.
What interventions are being tested in trial NCT00552695?
The interventions under investigation include: Placebo (DEVICE), Lidocaine tetracaine (DEVICE).
Who is sponsoring clinical trial NCT00552695?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00552695's enrollment target sits among peer trials
45 1296th of 2000 higher than 679 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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