Lumoptik BRIGHTPOINT Reflectometer Device for Lumbar Epidural Placement
Recruiting
Observational Study
Lumbar Spine Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 99
- Sex
- Any
- Study type
- Observational
- Participants needed
- 36 (estimated)
- Sponsor
- Hospital for Special Surgery, New York · Other
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About This Trial
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 t…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Any patient undergoing a lumbar neuraxial procedure requiring epidural needle
* Age 18-99
Exclusion Criteria:
* Previous lumbar spine surgery
* Any known spinal abnormality that would interfere with successfully advancing a needle into the epidural space
* Any patient requir…
Contacts