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NCT00126919 · ClinicalTrials.gov registry record · Phase 4
Reduction of Topical Anesthetic Time for Subcutaneous Port Access Using Ultrasound
A Phase 4 study, sponsored by Connecticut Children's Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 40
- Enrollment target
NCT00126919 is a Phase 4 study that has completed, run by Connecticut Children's Medical Center. The registered enrollment target is 40 participants.
The verdict
NCT00126919, a Phase 4 study, has completed, sponsored by Connecticut Children's Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 40 participants
- Enrollment target
Study Summary
Children ages 3-17 who are undergoing port access receive both standard care, topical medicine for numbing (LMX4), and the study intervention which utilizes ultrasound to speed the onset of LMX4 from 30 minutes to 5 minutes. The procedures will be performed on 2 separate visits to the clinic. The child's pain with the access procedure is evaluated.
Interventions
- DEVICE SonoPrep
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2004-10 |
| Est. Completion | 2006-10 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00126919
The ClinicalTrials.gov registry entry for NCT00126919 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Connecticut Children's Medical Center, which has 55 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which SonoPrep is the first listed.
NCT00126919 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00126919 about?
NCT00126919 is a clinical study titled "Reduction of Topical Anesthetic Time for Subcutaneous Port Access Using Ultrasound". Children ages 3-17 who are undergoing port access receive both standard care, topical medicine for numbing (LMX4), and the study intervention which utilizes ultrasound to speed the onset of LMX4 from 30 minutes to 5 minutes. The procedures will be performed on 2 separate visits to the clinic. The ch...
What is the current status of trial NCT00126919?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2004-10. Estimated completion is 2006-10.
What interventions are being tested in trial NCT00126919?
The interventions under investigation include: SonoPrep (DEVICE).
Who is sponsoring clinical trial NCT00126919?
This trial is sponsored by Connecticut Children's Medical Center, which has 55 total clinical trials registered on ClinicalTrials.gov.
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