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NCT02321787 · ClinicalTrials.gov registry record · NA
Ultrasonography for Confirmation of Caudal Injection
A NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT02321787 is a NA study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 100 participants.
The verdict
NCT02321787, a NA study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
The purpose of our study is to evaluate whether utilizing ultrasound assessment during caudal epidural injection can reliably identify unrecognized and unsuccessful nerve blocks during the procedure, guide proper technique, and alter pain management outcome measurements for patients. Patients will be randomized to a group either undergoing caudal injection by a trainee using typical techniques or by using typical techniques in addition to ultrasound for confirmation of successful injection. The patients enrolled in this study will have the same intraoperative care, in line with the standard of care. Data will be collected intraoperatively and postoperatively on pain scores, time for performance of caudal block, and perceived success of the block. There will be no direct benefit to the patients enrolled in this study, but future patients may benefit from the use of ultrasound for the confirmation of a successful block.
Interventions
- PROCEDURE Ultrasound for confirmation of successful caudal block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2014-12 |
| Est. Completion | 2015-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02321787
The ClinicalTrials.gov registry entry for NCT02321787 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Ultrasound for confirmation of successful caudal block is the first listed.
NCT02321787 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02321787 about?
NCT02321787 is a clinical study titled "Ultrasonography for Confirmation of Caudal Injection". The purpose of our study is to evaluate whether utilizing ultrasound assessment during caudal epidural injection can reliably identify unrecognized and unsuccessful nerve blocks during the procedure, guide proper technique, and alter pain management outcome measurements for patients. Patients will ...
What is the current status of trial NCT02321787?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2014-12. Estimated completion is 2015-10.
What interventions are being tested in trial NCT02321787?
The interventions under investigation include: Ultrasound for confirmation of successful caudal block (PROCEDURE).
Who is sponsoring clinical trial NCT02321787?
This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.
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