Clinical Trial: BrightPoint Reflectometer Device Study
Study Status: COMPLETED
Recruit Status: COMPLETED
Condition: Epidural Placement
Study Type: INTERVENTIONAL
Official Title: Human Clinical Trial to Evaluate the BRIGHTPOINT Reflectometer Device as Secondary Confirmation to Loss of Resistance in Lumbar Epidural Placement
Brief Summary:
Participants are being asked to participate in this study because they are having an epidural placed for labor.This human clinical trial has been designed to evaluate the use of the BrightPoint Reflectometer Device (AKA BrightPoint device) as secondary confirmation of Loss of Residence (LOR) for lumbar epidural placement by an experienced clinician.For this study, participants will be randomized to receive an epidural by an experienced clinician either with or without the use of the BrightPoint device.Epidurals…
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