New device aims to take the guesswork out of epidurals
NCT ID NCT04630171
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether a device called VerTouch can help doctors find the best spot for epidural or spinal anesthesia more accurately than using touch or ultrasound. Researchers compared the number of needle adjustments needed with each method in 86 adults undergoing these procedures. The goal is to make the process faster and less painful for patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- VerTouch device
- What this could lead to
- If it works well, this device could make epidural and spinal procedures quicker and more comfortable for patients.
- What could go wrong
- This is a small, completed study with 86 participants, so results may not apply to everyone. The device may not be better than current methods.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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86 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Nov 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients 18 years old and above * Undergoing a neuraxial procedure Exclusion Criteria: * Non English speaking * Plastic allergy * Unable to provide written informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Northwestern Memorial Hospital and Prentice Women's Hospital
Chicago, Illinois, 60611, United States
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