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NCT00126932 · ClinicalTrials.gov registry record · Phase 4
Reduction of Topical Anesthetic Onset Time Using Ultrasound
A Phase 4 study, sponsored by Connecticut Children's Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 70
- Enrollment target
NCT00126932: Completed Phase 4 study, sponsored by Connecticut Children's Medical Center.
NCT00126932 is a Phase 4 study that has completed, run by Connecticut Children's Medical Center. 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.
The verdict
NCT00126932, a Phase 4 study, has completed, sponsored by Connecticut Children's Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 70 participants
- Enrollment target
Study Summary
Children ages 3-7 who are undergoing blood drawing receive either standard care, topical medicine for numbing (LMX4), or the study intervention which utilizes ultrasound to speed the onset of LMX4 from 30 minutes to 5 minutes. The child's pain with the blood drawing procedure is evaluated.
Interventions
- DEVICE SonoPrep
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2004-10 |
| Est. Completion | 2004-12 |
| Phase | Phase 4 |
What the finished NCT00126932 record still lists
NCT00126932 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 1 intervention - of which SonoPrep is the first listed.
NCT00126932 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00126932 about?
NCT00126932 is a clinical study titled "Reduction of Topical Anesthetic Onset Time Using Ultrasound". Children ages 3-7 who are undergoing blood drawing receive either standard care, topical medicine for numbing (LMX4), or the study intervention which utilizes ultrasound to speed the onset of LMX4 from 30 minutes to 5 minutes. The child's pain with the blood drawing procedure is evaluated.
What is the current status of trial NCT00126932?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2004-10. Estimated completion is 2004-12.
What interventions are being tested in trial NCT00126932?
The interventions under investigation include: SonoPrep (DEVICE).
Who is sponsoring clinical trial NCT00126932?
This trial is sponsored by Connecticut Children's Medical Center, which has 55 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00126932'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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