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Study identifier: NCT06020508 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Lumoptik BRIGHTPOINT Reflectometer Device for Lumbar Epidural Placement

Condition: Lumbar Spine Surgery  ·  Sponsor: Hospital for Special Surgery, New York

PhaseN/A
Planned participants36
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to test the BrightPoint Epidural device as the first system to use multispectral reflectometry to find the epidural space in lumbar neuraxial procedures requiring epidural needle. The main questions it aims to answer are: 1. Is the device a qualitatively effective secondary confirmation of Loss of Resistance? 2. Is the device a qualitatively effective training tool for educating trainees in how to perform lumbar epidurals? Participants will undergo a neuraxial procedure in which the attending anesthesiologist will use the BrightPoint epidural device to form an opinion on its effectiveness in confirming epidural space access.

This description comes directly from the study's public registry record.

Talk to the study team

Pa Thor, PhD  ·  646-797-8535  ·  thorp@hss.edu

Maya Tailor  ·  646-714-6828  ·  tailorm@hss.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital for Special SurgeryNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06020508