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NCT01182220 · ClinicalTrials.gov registry record
Comparison of Ultrasound Guided Low Epidural Catheter Placement With Standard Epidural Catheter Placement
A clinical trial, sponsored by University of Chicago.
- Completed
- Registry status
- 90
- Enrollment target
NCT01182220: Completed study, sponsored by University of Chicago.
NCT01182220 is a clinical trial that has completed, run by University of Chicago. The registered enrollment target is 90 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01182220 has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- 90 participants
- Enrollment target
Study Summary
1. labor epidural quite often require bolus supplementation for better pain control control. Quite often this is due to sparing of sacral nerves. 2. If epidural is placed low in the L5/S1 interspace using ultrasound, this may minimize bolus requirement and improve patient labor experience.
Primary Outcome
After test dose and loading up of catheter, s1 and s2 dermatome blockage will be tested in L5/S1 epidural group vs conventionally placed epidural group. Idea is see if higher incidence of S1 and S2 blockage can be demonstrated in low epidural group.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2013-01 |
| Est. Completion | 2015-07 |
What the finished NCT01182220 record still lists
NCT01182220 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 90 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT01182220 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01182220 about?
NCT01182220 is a clinical study titled "Comparison of Ultrasound Guided Low Epidural Catheter Placement With Standard Epidural Catheter Placement". 1. labor epidural quite often require bolus supplementation for better pain control control. Quite often this is due to sparing of sacral nerves. 2. If epidural is placed low in the L5/S1 interspace using ultrasound, this may minimize bolus requirement and improve patient labor experience.
What is the current status of trial NCT01182220?
This trial is currently completed. The enrollment target is 90 participants. The study started on 2013-01. Estimated completion is 2015-07.
Who is sponsoring clinical trial NCT01182220?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
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